Emergency Department Nurse Jobs in Belgium, Wisconsin

Work Life Balance

Registered Nurse

DaVita Inc. Town of Belgium, WI

Registered Nurse page is loaded## Registered Nurseremote type: On-Sitelocations: 04473 - Brevard Dialysistime type: Full timeposted on: Posted 30+ Days Agojob requisition id: R0424724**Posting Date**09/22/2025102 College Station Dr Ste 10, Brevard, North Carolina, 28712, United States of America**Take the first step and apply now! Please ensure that you upload a resume with the most up to date work history.**If you haven't considered Nephrology before, read on as we think that you should.DaVita – which is Italian for "giving life" – is working to provide quality service to patients, partners, and teammates. Our mission is to be the Provider, Partner, and Employer of Choice.**Details about paid training and work schedule:*** **No Dialysis experience is required.*** Shifts: Three (12+ hour ) shifts with a minimum of two Saturdays/month with a starting time of 5:00 am. You must have a flexible schedule to be able to work mornings, evenings, Saturdays and holidays and at other locations nearby. The training may take place at your facility or another location* **Requirements:*** Associate’s degree in nursing (A.D.N) from accredited school of nursing required; three-year diploma from accredited diploma program may be substituted for nursing degreeWhat you can expect:* Build meaningful and long-term relationships with patients and their family in an intimate outpatient setting.* Be a part of a team that supports and relies on each other in a positive environment.* Deliver care to patients who are often dealing with multiple co-morbidities which require unique treatment plans and the ability to leverage a broad range of nursing skills and knowledge.* Oversee a group of patients with the support of PCTs to conduct patient observations, measuring stats and machine set up.* You will work with your head, heart and hands each day in a fast paced environment.What we'll provide:DaVita Rewards package connects teammates to what matters most including:* Comprehensive benefits: Medical, dental, vision, 401(k) match, paid time off, PTO cash out* Support for you and your family: family resources, EAP counseling sessions, access Headspace, backup child and elder care, maternity/paternity leave, pet insurance, and more* Paid trainingDaVita is a clinical leader! We have the highest percentage of facilities meeting or exceeding CMS's standards in the government's two key performance programs. We expect our nurses to commit to improving patient health through clinical goal setting and quality improvement initiatives.#LI-CH3At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and comply with state and federal affirmative action requirements. Individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.This position will be open for a minimum of three days.For location-specific minimum wage details, see the following link:Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies and experience. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at **Colorado Residents: Please do not respond to any questions in this initial application that may seek age-identifying information such as age, date of birth, or dates of school attendance or graduation. You may also redact this information from any materials you submit during the application process. You will not be penalized for redacting or removing this information.**DaVita (NYSE: DVA) is a comprehensive kidney care provider focused on transforming care to improve the quality of life for patients globally. The company is a leading provider of kidney care services in the U.S. and has been a leader in clinical quality and innovation for more than 20 years. DaVita is working to help increase equitable access to care for patients at every stage and setting along their kidney health journey—from slowing progression of kidney disease to streamlining the transplant process, from acute hospital care to dialysis at home. As of March 31, 2022, DaVita served 200,800 patients at 2,809 outpatient dialysis centers in the U.S. The company operated an additional 346 outpatient dialysis centers in 11 other countries worldwide. DaVita has reduced hospitalizations, improved mortality and worked collaboratively to help propel the kidney care community to adopt an equitable, high-quality standard of care for patients around the globe.To learn more about what it means to be a part of our Village, visit .DaVita is an equal opportunity employer- Male/Female/Veterans/Disabled. To learn more about what this means click .We maintain a drug-free workplace and perform pre-employment substance abuse testing and background verification checks. We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws.#J-18808-Ljbffr

Dynamic Environment

Regional Nurse Educator

AmerisourceBergen Town of Belgium, WI

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Qualifications Masters' education is preferred Oncology experiences an asset Experience with research an asset member of a nursing association preferred CPR required Comfort with working on online platforms and virtual teaching Teaching experience preferred Primary Duties and Responsibilities Accountable for creation and ongoing development of training standards, documents, policies and processes for any new initiatives in collaboration with Nursing leadership. Acts as a resource for all Field Nurses and BAMs to grow in proficiency and confidence regarding molecule specific standard operating procedures, work instructions and disease state understanding by providing clinical guidance to Field Nurses to make the adoption of new knowledge, information and best practices integrated into real time patient care delivery with a focus on PSPs and ICP. Participates regularly in telephone consultations and/or web based meetings/training sessions with Field Nurses within their geographical area or across Canada. Develops expert knowledge on the administration of biologics, specialty biologics, biosimilars and specialty generic drugs by actively participating in all launch and client-provided education seminars as well as self-directed study, with a focus on disease state and clinical skill. On a quarterly basis, collaborates with designated BAM/IBU to assess training needs specific to that IBU/region and/or nationally across Canada, and then creates and delivers training, including remedial training plans or re-training of nurses returning from leave In collaboration with the Nursing Leadership team, develops and implements patient education tools, nursing educational materials, nursing competency assessment tools, evaluation tools and critical thinking case studies reflecting evidence informed practices that support remote learning Works collaboratively with other Regional Nurse Educators and Business Area Managers to support Innomar’s Field Nurse Preceptorship program by providing tools and training to new Preceptors, participating in the selection of nurses for preceptor roles Responsible for the design and ongoing development of competency requirements for Innomar’s Field Nurse Preceptorship program, in collaboration with Business Area Managers, and contributes to the ongoing evaluation of preceptors in their role Works collaboratively with peers and other departments to ensure efficiencies are realized with product and disease state training for each new molecule launch, including decision-making for cost-effective nursing supplies and practices Drives standardization of nursing practice and processes through ongoing research into best practices, and takes leadership in the development of nursing Policies, Standard Operating Procedures, Work Instructions and Forms Takes leadership in creation of Quality and Best Practice cross-functional committees, terms of reference and agendas to support interdisciplinary collaboration and decision-making on best nursing practices for Innomar Works collaboratively with other Regional Nurse Educators and Business Area Managers to review CAPAs, attend or review audits, review incident reports and patient complaints to determine training gaps and recommend practice solutions In collaboration with the BAM, participates remotely in recruitment interviews of Field Nurses, providing input into skills assessments and learning plans Attends therapeutic area conferences based on business needs, and presents at conferences based on subject matter expertise, as appropriate In partnership with DNOs and BAMs, supports KOLs and drives Innomar’s brand presence through delivery of patient education to their therapeutic patient groups, based on own subject matter expertise Acts as a resource to clients to support new initiatives or fill training gaps identified by the client. Acts as the face of the organization through appearance, attitude, and communication when in client and professional settings, such as conferences, train the trainer sessions, and meetings with KOLs etc. Monitors updates within provincial legislations, clinical requirements and industry trends Actively participates in Nursing team and interdepartmental meetings At times may be called upon to consult with physicians, pharmaceutical and biotechnology clients regarding education and implementation of product specific programs Flexibility in order to provide services for pre-scheduled meetings, training sessions, mentorship/support activities, and occasional last‑minute requests, in‑person, via teleconference, when required be available to travel to attend in‑person Innomar office meetings and other meeting locations. Adheres to professional nursing standards as prescribed by the professional associations and the company Develops and demonstrates expanding expertise in all therapeutic areas of interest to Innomar Performs related duties and tasks as required May be required to be on standby/ on call as part of this role Experience and Educational Requirements Qualified registered nurse in the province of residence (valid provincial license from the College of Nurses) Healthcare provider CPR certificate required Minimum 5 years’ experience as a Registered Nurse with experience being a nurse educator, clinical resource to other health care professionals 3 years of regular IV initiation and infusion experience Experience in a critical care, emergency, acute care inpatient/outpatient or homecare setting are considered assets ACLS, CVAA Certification, and central venous line/port experience are required Specialty certifications in therapeutic areas such as oncology and immunology are an asset Possess a valid driver’s license, access to a reliable vehicle, and car insurance Minimum Skills, Knowledge, and Ability Requirements Exceptional ability to communicate effectively both orally and in writing Effective interpersonal and leadership skills Effective organizational skills; attention to detail Strong ability to consistently meet deadlines and prioritize Excellent problem‑solving skills; ability to resolve issues effectively and efficiently Excellent presentation skills Bilingual skills an asset Knowledge of Microsoft Word, Excel, PowerPoint and other Office Programs Ability to Travel Able to work autonomously with little supervision Makes decisions using sound clinical judgment and takes initiative with minimal direction Manages multiple competing priorities to meet established deadlines demonstrating organizational savvy, business acumen and quality work/project results. What Cencora offers We provide compensation, benefits, and resources that enable a highly inclusive culture and support our team members’ ability to live with purpose every day. In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness. This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more. Full time Equal Employment Opportunity Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law. The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non‑discriminatory. Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email [email protected]. We will make accommodation determinations on a request‑by‑request basis. Messages and emails regarding anything other than accommodations requests will not be returned Accessibility Policy Cencora is committed to fair and accessible employment practices. When requested, Cencora will accommodate people with disabilities during the recruitment, assessment and hiring processes and during employment. Affiliated Companies Affiliated Companies: Innomar Strategies #J-18808-Ljbffr

Work Life Balance

Registered Nurse - Work In Ireland - Fully Paid Relocation Package

Mercier Consultancy Europe Town of Belgium, WI

Registered Nurse – Work In Ireland – Fully Paid Relocation Package Mercier Consultancy Europe is pleased to offer an exciting opportunity for Registered Nurses who are eager to work in Ireland. This role includes a fully paid relocation package, and offers a competitive monthly salary. We are looking for dedicated and compassionate nursing professionals who are ready to provide high‑quality patient care in a dynamic healthcare setting. Key Responsibilities Conduct thorough patient assessments and develop personalized care plans. Administer medications and treatments in compliance with established protocols and physician orders. Continuously monitor and evaluate patient conditions, documenting vital signs and significant changes for the healthcare team. Educate patients and their families on health management, treatment options, and preventive care strategies. Maintain accurate records and documentation of all patient interactions in adherence to regulatory standards. Collaborate with multidisciplinary teams to ensure comprehensive patient care. Apply infection control and safety protocols to maintain a safe environment for patients and staff. Requirements Bachelor’s degree in Nursing with valid registration as a Registered Nurse in your home country, or eligibility for nursing registration in Ireland. Proficient in English with excellent verbal and written communication skills. Previous nursing experience in a clinical or hospital setting is desirable. Strong commitment to providing high‑quality, compassionate patient care. Ability to work collaboratively in a team‑oriented healthcare environment. Exceptional organizational and time‑management skills. Willingness to relocate to Ireland and adapt to a new cultural and professional landscape. Benefits Competitive monthly salary. Fully paid relocation package. Fully paid training. Health insurance. And more. #J-18808-Ljbffr

Staff - Registered Nurse (RN) - Home Health Case Management - $37-56 per hour

RemoteWorker US Town of Belgium, WI

Advocate Aurora Health is seeking a Registered Nurse (RN) Home Health Case Management for a nursing job in Belgium, Wisconsin. Job Description & Requirements Specialty: Case Management Discipline: RN Duration: Ongoing 32 hours per week Shift: days Employment Type: Staff Major Responsibilities: Assumes responsibility for caseloads consisting of patients in specialty areas. Conducts initial assessment to obtain thorough physical, social and environmental data. Establishes the plan of care in accordance with the physician orders and patient needs. Provides direct patient care and adjusts nursing care processes as needed. Identifies problems, modifies nursing care plan, and evaluates outcomes within an appropriate time frame. Advises and consults with family and other personnel, as appropriate. Provides on-going assessment of patient response to treatments and teaching and applies interventions as appropriate. Updates and revises plan of care as indicated. Completes documentation including visit assessment, OASIS, 485 and verbal orders accurately and promptly and within the standards. Communicates with physicians to confirm and update patients' plan of care. Provides status updates and ensures ongoing communication with the physician and other members of the health care team. Facilitates the discharge planning process according to standards and utilizes resources to assure continuity of care after discharge. Participates in developing the discharge plan with the patient/family, physician, social worker, and other staff members as appropriate. Participates in chart audits and continuous quality improvement activities as requested. Identifies, develops and participates in process improvement opportunities that will enhance the quality of the services provided. Maintains and updates accurate clinical and patient records according to agency, state, and federal guidelines. Must be able to demonstrate knowledge and skills necessary to provide care appropriate to the age of the patients served. Must demonstrate knowledge of the principles of growth and development over the life span and possess the ability to assess data reflective of the patient's status and interpret the appropriate information needed to identify each patient's requirements relative to his/her age-specific needs, and to provide the care needed as described in the department's policies and procedures. Age-specific information is developed further in the departmental job standards. Licensure, Registration, and/or Certification Required: Registered Nurse license issued by the state in which the team member practices, and Basic Life Support (BLS) for Healthcare Providerscertification issued by the American Heart Association (AHA) needs to be obtained within 6 months unless department leader has determined it is not required, and A valid drivers license issued by the Division of Motor Vehicles, or Driver license issued by the state of Illinois. Education Required: Associate's Degree in Nursing. Experience Required: Typically requires 3 years of experience in clinical nursing. Knowledge, Skills & Abilities Required: Excellent communication skills. Strong interpersonal skills and the ability to work with a variety of clients with patience and respect. Good organizational, analytical and problem solving skills. Demonstrated ability to work well with physicians and other professionals in a direct and positive manner. Proficiency in clinical skills with the ability to work under direction and make sound judgments. Ability to operate the necessary equipment to perform the job, i.e., FAX, computer, copier, telephone system. Ability to assess data reflecting the patient's status and the ability to interpret the appropriate information needed to identify each patient's requirements relative to their specific needs. Must have a tolerance for differences and an appreciation of multi-culturalism and diversity of the patients and their families. Must possess and provide proof of a valid Driver License and a registered, functional car with adequate insurance coverage. Physical Requirements and Working Conditions: Must be capable of the manual dexterity required to use and operate a variety of equipment. Must have the physical ability to move about in confined spaces, including bending, twisting, kneeling, squatting and occasionally reaching one or both arm overhead. Must be able to work safely with people of various sizes and weight with diverse and complex medical conditions and physical limitations. Must be able to sit, stand, walk and climb stairs for limited to prolonged periods of time to complete required paperwork, gain entry to patients’ residences, travel from assigned visits and attend a variety of work related activities. Must have the physical stamina to attend to patient care requirements over a period of three or more hours without complete rest. Must have accurate vision to read gauges and measuring devices and to interpret written instructions. Subject to extreme temperature changes due to weather conditions. Subject to exposure to chemical and hazardous waste and communicable disease. Must be able to: Lift up to 50 lbs from floor to waist. Lift up to 20 lbs from waist to overhead. Lift and carry up to 40 lbs. at waist height reasonable distance. Must be able to: Push/pull with 30 lbs. of force. Perform a sliding transfer of 150 lbs. with a second person present. This job description indicates the general nature and level of work expected of the incumbent. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the incumbent. Incumbent may be required to perform other related duties. Advocate Aurora Health Job ID #R142136. Posted job title: Home Health RN Case Manager - Grafton area About Advocate Aurora Health Advocate Aurora Health’s 22,000 nurses demonstrate our values of excellence, compassion and respect, collaborating to advance our stated purpose of helping people live well. To encourage you to be the best nurse you can, Advocate Aurora will provide support, tools and resources for orientation, education and professional development, in the care setting that is best for you. Your voice as a team member will be heard clearly whether you’re at one of our 10 Magnet designated hospitals or more than 500 sites of care. Join our team and be inspired to chart a course for Advocate Aurora to become the best place in the nation for nurses to pursue their passion. Benefits Holiday Pay Guaranteed Hours Continuing Education 401k retirement plan Pet insurance Wellness and fitness programs Mileage reimbursement Employee assistance programs Medical benefits Dental benefits Vision benefits Life insurance Discount program #J-18808-Ljbffr

Quick Apply

LPN (Licensed Practical Nurse) Home Care - Sheboygan/Ozaukee Counties

Preceptor Home Health & Hospice Town of Belgium, WI

We are seeking a Home Health LPN Visit Nurse to provide care in Sheboygan and Ozaukee Counties!! At Preceptor Home Health and Hospice, we embrace an atmosphere of caring, belonging, and trust. You will enjoy meaningful connections that come from this culture, including with your patients and their families, each other, and the communities we serve. Preceptor strives to provide high quality care through our multifaceted programs. It is truly all about helping people and allowing you to build a meaningful career with us!! As a Home Health LPN, you can expect: To develop trusting relationships with patients, families, and your community Being valued and respected by patients and their families "Customer Second" support as part of our core CAPLICO values (Customer Second, Accountability, Passion for Learning, Love One Another, Intelligent Risk Taking, Celebration, and Ownership) Incredible team support and empathetic leadership The ability to take your nursing career to a new level of caring As the LPN Visit Nurse, you will provide quality care to our home health patients, working closely with the RN Case Manager. Duties include, but are not limited to: Performing routine nursing visits Providing wound care -- we take great pride in being a preferred provider for several local wound care clinics Providing catheter care Excellent communication skills with clients, families, doctors, facility staff, and co-workers is a must to be successful in this role Ability to work independently Good organization and time management skills are also critical Love working with the geriatric population Experience Requirements: One year of clinical experience preferred. License Requirements: Current Wisconsin LPN licensure Current driver\'s license, valid vehicle insurance, and access to a dependable vehicle Position Details: Location: Brown, Winnebago, and Calumet Counties Schedule: Full-Time, 1st shift Monday-Friday. Minimal on-call required. Compensation: $25-$30/hour based on experience. Why Choose Preceptor Home Health & Hospice? Comprehensive Benefits Package: Health, dental, vision, and life insurance Paid mileage for travel between patient visits Accrued Paid Time Off (PTO) and sick time Paid holidays 401(k) plan with employer contribution Professional Development: Small education stipend for qualifying staff Work-Life Balance: Flexible scheduling options to support your personal life. Minimal on call is required. We would love the opportunity to add you to our team! If you feel this is for you, please apply today! #J-18808-Ljbffr

Education Manager - Healthcare - Belgium

Dexcom Town of Belgium, WI

Education Manager - Healthcare - Belgium role at Dexcom Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom has pioneered the industry for 25 years and continues to empower people to take control of health through personalized, actionable insights. Responsibilities Support, train, and educate HCPs on Dexcom products in the Diabetes Market. Provide online and in-person training and in-servicing of Dexcom products and ancillaries to patients and HCPs in innovative ways. Develop innovative and efficient ways to set up an education platform utilizing support from across the company. Maximize strategic partnership with stakeholders to maximize sales for CGM products. Serve as the first point of contact for product, use, and training requests and questions by HCPs. Manage time according to customer and business needs. Qualifications 3+ years of experience training HCPs and/or patients. Excellent interpersonal skills; fluent in Dutch and French, and good knowledge of English. Preferably has experience working in the diabetes field. Has a (para) medical education at BSc. Level (e.g., nurse, dietician, physiotherapist). Benefits A front row seat to life-changing CGM technology; learn about the #dexcomwarriors community. A full and comprehensive benefits program. Growth opportunities on a global scale. Access to career development through in-house learning programs and/or qualified tuition reimbursement. An exciting and innovative, industry-leading organization committed to employees, customers, and the communities served. Travel 50-75% of time required. Experience & Education Typically requires a Bachelor’s degree and 5–8 years of related experience. Remote Workplace Your location will be a home office; a hybrid working environment may be available if you reside within commuting distance of a Dexcom site (typically 75 miles/120 km). Dexcom offers Flex workplace options. #J-18808-Ljbffr

Best Match

Medical Sales Representative Belgium

Resourcing Life Science Town of Belgium, WI

Responsibilities Support customers within the assigned region. Train healthcare professionals (nurses, physicians, therapists). Establish and nurture strong relationships with Key Opinion Leaders (KOLs) and other key stakeholders in the healthcare industry. Contribute to the development of training materials Represent the company at trade fairs, congresses, and professional training events. Gather and communicate customer feedback to drive continuous improvement of products and services. Qualifications Bachelor degree in life-science Min 1.5 year monitoring experience as Sales Rep in Medical devices or Pharma Ability to travel 75% Fluent English Excellent communication skills A full clean drivers license FTE: 1.0 #J-18808-Ljbffr

Brand Manager

GlaxoSmithKline Town of Belgium, WI

Job Purpose As Brand Manager, you will lead the commercialization of one or several ViiV products on a national level by developing and implementing the marketing strategy and operational marketing mix and tactics. You will have a pivotal role in order to meet the target sales objectives and the best possible market performance. Key Responsibilities LEADERSHIP: Advocate for, lead all activity and be accountable for the assigned brand. Embedding a winning mindset for the brand within the organization. INSIGHTS & EXPERT MARKET KNOWLEDGE: Continuously seek to understand and embed customer and market insights into all brand activities by synthesizing qualitative feedback from various sources (field visits, market research reports, customer conversations, Key Account Management feedback, etc) with quantitative feedback available through various data sources and reports. Be the product, competitor, and market expert aligned with assigned brand. BRAND PLANNING: Develop and implement annual strategic and operational brand plans through cross-functional collaboration (Commercial Manager, Medical Affairs Manager) and aligned with customer and market insights. Identify opportunities for business growth and competitive advantage. Define the national and/or international activities to support and improve the product performance (e.g. symposia, advisory board, meetings…) in close collaboration with the Medical Affairs Manager and the Commercial Manager. OPERATIONS / EXECUTION: Deliver promotional campaigns and all marketing materials within operational excellence and in alignment with LOC and above country guidelines, the ethical code and internal ground rules of ViiV. Advertising & Promotion (A&P) budgets are actively managed in close collaboration with the Finance Partner and Country Manager; FIELD ENGAGEMENT: Liaise very closely with the Commercial Manager and with the sales team to receive market and customer feedback, embed campaigns, and to provide brand vision. During cycle meetings, present the new developed materials and the new promotional messages to the Sales team. Ensure full understanding of the rationale and insights that underpin campaigns, messages, and marketing actions. Follow up with the Sales team how the materials and messages are accepted by the Healthcare providers, nurses and/or patients. DRIVE PERFORMANCE: Drive Brand Performance through the cross-functional team to maximize brand potential; deliver versus the agreed targets, actively pursue opportunities, minimise risk and ensure that course corrections are in place; EXTERNAL ENGAGEMENTS: Regularly gather customer insights and seek the feedback on marketing inputs and campaigns from External Experts, HCPs, nurses. BRAND EXPERTISE: Keep up his/her expertise on the ViiV products and on the competition as well as in terms of knowledge of the latest clinical data, strategic options and regulatory changes. Be the key contact person concerning the ViiV product he/she is responsible for; answer specific questions related to the product in close collaboration with Medical Affairs Manager. Why You? Basic Qualifications: Masters degree in Medical / Sciences or other relevant specialty. Prior pharmaceutical marketing/sales/medical experience preferred – 2 years minimum Fluent communication in English and Dutch. Good communication in French is a plus. Preferred Qualifications: Strong communication and engagement skills. Experience with brand planning processes and translating strategy into execution. Experience using multiple channels of marketing mix & evidence of successful implementations through digital channels. Ability to lead cross-functional matrix working. Happy to challenge others and accepts to be challenged him/herself. Ability to engage with opinion leaders and understand the stakeholder perspective. Flexible thinking and ability to continuously innovate and learn. #LI-GSK If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. #J-18808-Ljbffr

Brand Manager

Viiv Healthcare Town of Belgium, WI

Brand Manager page is loaded## Brand Managerlocations: Belgium-Wavretime type: Full timeposted on: Posted 2 Days Agojob requisition id: 429373# # **Job Purpose**# As Brand Manager, you will lead the commercialization of one or several ViiV products on a national level by developing and implementing the marketing strategy and operational marketing mix and tactics. You will have a pivotal role in order to meet the target sales objectives and the best possible market performance.# **Key Responsibilities*** LEADERSHIP: Advocate for, lead all activity and be accountable for the assigned brand. Embedding a winning mindset for the brand within the organization.* INSIGHTS & EXPERT MARKET KNOWLEDGE: Continuously seek to understand and embed customer and market insights into all brand activities by synthesizing qualitative feedback from various sources (field visits, market research reports, customer conversations, Key Account Management feedback, etc) with quantitative feedback available through various data sources and reports. Be the product, competitor, and market expert aligned with assigned brand.* BRAND PLANNING: Develop and implement annual strategic and operational brand plans through cross-functional collaboration (Commercial Manager, Medical Affairs Manager) and aligned with customer and market insights. Identify opportunities for business growth and competitive advantage. Define the national and/or international activities to support and improve the product performance (e.g. symposia, advisory board, meetings…) in close collaboration with the Medical Affairs Manager and the Commercial Manager.* OPERATIONS / EXECUTION: Deliver promotional campaigns and all marketing materials within operational excellence and in alignment with LOC and above country guidelines, the ethical code and internal ground rules of ViiV. Advertising & Promotion (A&P) budgets are actively managed in close collaboration with the Finance Partner and Country Manager;* FIELD ENGAGEMENT: Liaise very closely with the Commercial Manager and with the sales team to receive market and customer feedback, embed campaigns, and to provide brand vision. During cycle meetings, present the new developed materials and the new promotional messages to the Sales team. Ensure full understanding of the rationale and insights that underpin campaigns, messages, and marketing actions. Follow up with the Sales team how the materials and messages are accepted by the Healthcare providers, nurses and/or patients.* DRIVE PERFORMANCE: Drive Brand Performance through the cross-functional team to maximize brand potential; deliver versus the agreed targets, actively pursue opportunities, minimise risk and ensure that course corrections are in place;* EXTERNAL ENGAGEMENTS: Regularly gather customer insights and seek the feedback on marketing inputs and campaigns from External Experts, HCPs, nurses.* BRAND EXPERTISE: Keep up his/her expertise on the ViiV products and on the competition as well as in terms of knowledge of the latest clinical data, strategic options and regulatory changes. Be the key contact person concerning the ViiV product he/she is responsible for; answer specific questions related to the product in close collaboration with Medical Affairs Manager.**Basic Qualifications:*** Masters degree in Medical / Sciences or other relevant specialty.* Prior pharmaceutical marketing/sales/medical experience preferred – 2 years minimum* Fluent communication in English and Dutch. Good communication in French is a plus.**Preferred Qualifications:*** Strong communication and engagement skills.* Experience with brand planning processes and translating strategy into execution.* Experience using multiple channels of marketing mix & evidence of successful implementations through digital channels.* Ability to lead cross-functional matrix working.* Happy to challenge others and accepts to be challenged him/herself.* Ability to engage with opinion leaders and understand the stakeholder perspective.* Flexible thinking and ability to continuously innovate and learn.#LI-GSKIf you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.**Uniting science, technology and talent to get ahead of disease together.**GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.**Important notice to Employment businesses/ Agencies**GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.At **ViiV Healthcare**, we will not rest until we leave no person living with HIV behind. Until the 39 million people living with HIV is down to zero, we will continue searching for new ways to limit the impact of HIV.We are the only pharmaceutical company solely focused on combating, preventing, and ultimately eradicating HIV and AIDS. At **ViiV Healthcare**, we do things differently. Born out of a partnership between and in 2009, with joining in 2012, we are determined to help end the HIV epidemic. We are guided by our mission to leave no person living with HIV behind and it is this mission that unites our employees located across the globe. We combine expertise in research, manufacturing, policy and more to push the boundaries of what people think is possible in HIV treatment and care. As a result of our connection with GSK, we are able to draw on their proud history and resources. This means that you would receive all the employee benefits offered by GSK.Living our mission of leaving no person living with HIV behind means keeping inclusion and diversity at the heart of everything we do - from our breakthrough innovation, to our diverse portfolio of medicines as well as the work we do to partner with HIV communities. Having a diverse team and a truly inclusive culture where we’re all able to be ourselves and feel like we belong will make us an even stronger team, better able to perform as a business and deliver on our mission to leave no person living with HIV behind.#J-18808-Ljbffr

Patient Care Technician

DaVita Inc. Town of Belgium, WI

**Posting Date**09/16/20251711 Alton Rd, Miami Beach, Florida, 33139-2411, United States of AmericaIf you haven't considered Nephrology before, read on as we think that you should.Joining DaVita as Patient Care Technician (PCT) is an exciting opportunity to jump start your career in the health care industry! With paid, extensive training, you will gain the skills needed to care for our patients and build a network of other health care professionals across the geography where you live. Once you have successfully completed training, you will join a holistic team of care professionals – including nurses, dietitian, social workers, and other experienced PCTs – to care for our patients. It's not a job, it's giving life and a career based on passion and purpose.DaVita – which is Italian for "giving life" – is working to provide quality service to patients, partners, and teammates. Our mission is to be the Provider, Partner, and Employer of Choice.Our PCTs also find DaVita professionally fulfilling. To help advance your career, we offer clear paths to higher levels of responsibility and compensation through our Clinical Ladders program. Through DaVita's Bridge to your Dreams program, teammates who have been in their role for six consecutive months and in good standing, are eligible to receive tuition assistance up front to pursue their dream of becoming a DaVita RN and getting their Associates Degree in Nursing. We also have dedicated training to become a Facility Administrator, and training to become a Regional Operations Director. Your success is driven by your performance and desire.Some details about this position:* No Dialysis experience is required.* Training may take place in a facility or a training clinic other than your assigned home clinic* Potential to float to various clinics during and after your training* You must have a flexible schedule and be able to work mornings, evenings, weekends, and holidaysWhat you can expect:* Direct Patient Care. Spend the majority of your day in direct one-on-one patient care to provide safe, comfortable and hygienic dialysis treatment.* Our PCTs care for multiple patients.* Technician Duties. To monitor patients before, during and after dialysis treatment including measuring and recording stats, patient observations, and hemodialysis machine setup. Please note you will have exposure to blood and needles.* Building long-term relationships with your patients who are suffering from end stage renal disease and are receiving treatment on average 3 times/week. You will also be responsible for educating patients on Kidney Dialysis related topics.* Team. Cross functional team of clinicians including technicians, nurses, dietitians, social workers and leadership. PCTs work under the supervision of a RN.What we'll provide:DaVita Rewards package connects teammates to what matters most including:* Comprehensive benefits: Medical, dental, vision, 401(k) match, paid time off, PTO cash out* Support for you and your family: family resources, EAP counseling sessions, access Headspace, backup child and elder care, maternity/paternity leave, pet insurance, and more* Paid trainingRequirements:* Desire to enter the health care field to care for other people in need* High school diploma or equivalent* Must be comfortable working around blood and needles* Must be comfortable mixing acid or bicarb* Physical and mental ability to work long hours (some shifts are 12+ hours) on your feet so wear comfortable shoes! Our work ends when it's safe for our patients.* Willingness to train and work across multiple clinics within the territory as needed.* Health care experience a plus including: BONENT Certified, Certified Hemodialysis Technician (CHT), Certified Nursing Assistant (CNA), Certified Medical Assistant (CMA), or Phlebotomy certification.DaVita is a clinical leader! We have the highest percentage of facilities meeting or exceeding CMS's standards in the government's two key performance programs. We expect our teammates to commit to improving patient health through clinical goal setting and quality improvement initiatives.#LI-LK3At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and comply with state and federal affirmative action requirements. Individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.This position will be open for a minimum of three days.For location-specific minimum wage details, see the following link:Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies and experience. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at **Colorado Residents: Please do not respond to any questions in this initial application that may seek age-identifying information such as age, date of birth, or dates of school attendance or graduation. You may also redact this information from any materials you submit during the application process. You will not be penalized for redacting or removing this information.**DaVita (NYSE: DVA) is a comprehensive kidney care provider focused on transforming care to improve the quality of life for patients globally. The company is a leading provider of kidney care services in the U.S. and has been a leader in clinical quality and innovation for more than 20 years. DaVita is working to help increase equitable access to care for patients at every stage and setting along their kidney health journey—from slowing progression of kidney disease to streamlining the transplant process, from acute hospital care to dialysis at home. As of March 31, 2022, DaVita served 200,800 patients at 2,809 outpatient dialysis centers in the U.S. The company operated an additional 346 outpatient dialysis centers in 11 other countries worldwide. DaVita has reduced hospitalizations, improved mortality and worked collaboratively to help propel the kidney care community to adopt an equitable, high-quality standard of care for patients around the globe.To learn more about what it means to be a part of our Village, visit .DaVita is an equal opportunity employer- Male/Female/Veterans/Disabled. To learn more about what this means click .We maintain a drug-free workplace and perform pre-employment substance abuse testing and background verification checks. We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws.#J-18808-Ljbffr

Regulatory and Start Up Specialist/ Senior Regulatory and Start Up Specialist

Precision for Medicine Town of Belgium, WI

Regulatory and Start Up Specialist / Senior Regulatory and Start Up Specialist Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life‑changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. As our organisation continues to grow we are hiring a Regulatory and Start Up Specialist / Senior Regulatory and Start Up Specialist to join our team in Belgium or The Netherlands. This position can be only offered fully home based. Essential Functions Responsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks for Belgium and The Netherlands. Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to CA, EC, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH‑GCP. Interaction with CA/EC for study purposes and handling responses to the CA/EC. Providing regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership Preparation/Support the development of study specific start‑up plans, IMP release requirements and essential document review criteria. Partner with the assigned site CRA to ensure alignment in communication and secure site review and manage collection of essential documents required for site activation/IMP release. Customize country/site specific Patient Information Sheet and Informed Consent Form. Responsible for/facilitates the translation and co‑ordination of translations for documents. Maintain communication with other key functions participating to country start up e., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group on project specific status and deliverables. Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements for and other required reviews to secure on time site activation for the assigned sites in the country. When required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department. May participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study. Keep an updated knowledge of the local clinical trial laws, regulations and help distributing their knowledge within PFM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations. Maintain audit/inspection readiness at all times and file documents as per TMF plan and/ or study specific plans in the relevant TMF May support the clinical team performing Pre‑Study Site Visits. Experience / Qualifications Bachelor’s degree in life sciences or related field (ideally in a scientific or healthcare discipline), or Registered Nurse (RN) or equivalent combination of education, training, and experience. 1 year or more as a Regulatory or SU specialist (or comparable role) in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. 1 year or more in part II submissions for clinical trials in Belgium and/or Netherlands 1 year or more for ICF country adaptation for Belgium and/or Netherlands 1 year or more in site level documents collection for submissions and IP release for Belgium and/or Netherlands Regulatory/ SU experience for covering Belgium and the Netherland Fluency in Dutch and English Fluency in French is a plus Other Required Strong communication and organizational skills. Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. Preferred Experience using milestone tracking tools/systems. Ability to prioritize workload to meet deadlines Advanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science. We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected] . #J-18808-Ljbffr

Regulatory and Start Up Specialist/ Senior Regulatory and Start Up Specialist

Precision Medicine Group Town of Belgium, WI

Regulatory and Start Up Specialist / Senior Regulatory and Start Up Specialist 2 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life‑changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences. As our organisation continues to grow we are hiring a Regulatory and Start Up Specialist / Senior Regulatory and Start Up Specialist to join our team in Belgium or The Netherlands. This position can only be offered fully home based. Essential functions of the job include but are not limited to: Preparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to CA, EC, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH‑GCP. Interaction with CA/EC for study purposes and handling responses to the CA/EC. Providing regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team. Maintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership. Preparation/Support the development of study specific start‑up plans, IMP release requirements and essential document review criteria. Partner with the assigned site CRA to ensure alignment in communication and secure site. Review and manage collection of essential documents required for site activation/IMP release. Customize country/site specific Patient Information Sheet and Informed Consent Form. Responsible for/facilitates the translation and co‑ordination of translations for documents. Maintain communication with other key functions participating to country start up (e.g., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group) on project specific status and deliverables. Act as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements for and other required reviews to secure on time site activation for the assigned sites in the country. When required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department. May participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study. Keep an updated knowledge of the local clinical trial laws, regulations and help distributing their knowledge within PFM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations. Maintain audit/inspection readiness at all times and file documents as per TMF plan and/or study specific plans in the relevant TMF. May support the clinical team performing Pre‑Study Site Visits. Experience / Qualifications Minimum Required Bachelor’s degree in life sciences or related field (ideally in a scientific or healthcare discipline), or Registered Nurse (RN) or equivalent combination of education, training, and experience. 1 year or more as a Regulatory or SU specialist (or comparable role) in either a CRO or pharmaceutical/biotech industry or equivalent, relevant experience and/or demonstrated competencies. 1 year or more in part II submissions for clinical trials in Belgium and/or Netherlands. 1 year or more for ICF country adaptation for Belgium and/or Netherlands. 1 year or more in site level documents collection for submissions and IP release for Belgium and/or Netherlands. Regulatory/ SU experience for covering Belgium and the Netherlands. Fluency in Dutch and English. Fluency in French is a plus. Other Required Strong communication and organizational skills. Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. Preferred Experience using milestone tracking tools/systems. Ability to prioritize workload to meet deadlines. Advanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science. We invite you to learn more about our growing organization serving our clients that are researching ground‑breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company. Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, please contact Precision Medicine Group at [email protected]. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process. #J-18808-Ljbffr

Social Worker

DaVita Inc. Town of Belgium, WI

Social Worker page is loaded## Social Workerremote type: On-Sitelocations: 02141 - Commerce Townshiptime type: Part timeposted on: Posted 16 Days Agojob requisition id: R0427886**Posting Date**10/14/2025120 W Commerce Rd, Commerce Township, Michigan, 48382, United States of AmericaAs a Social Worker at DaVita, you’ll be a part of a Team that values work-life balance and where your personal and professional growth is a top priority.DaVita has an open position for a Social Worker who will be a vital member of each patient’s core care team. Life on dialysis can be a difficult transition for many patients-and you'll be there to support and advocate for them. In this vital role, you will help patients understand their rights and responsibilities, and guide them in managing the physical, mental, emotional and financial demands of End Stage Renal Disease.If you love patient-centered health care and knowing patients on a personal level—now is your time to explore your next journey—at DaVita.What you can expect:* Build meaningful and long-term relationships with patients and their families in an intimate outpatient setting.* Be a part of a Team that appreciates, supports and relies on each other in a positive environment.* Performance-based rewards based on stellar individual and team contributions.What we'll provide:DaVita is a clinical leader! We have the highest percentage of facilities meeting or exceeding CMS's standards in the government's two key performance programs. We expect our nurses to commit to improving patient health through clinical goal-setting and quality improvement initiatives.Comprehensive benefits:* DaVita offers a competitive total rewards package to connect teammates to what matters most.* We offer medical, dental, vision, 401k match, paid time off, PTO cash out, paid training and more.* DaVita provides the opportunities for support for you and your family with family resources, EAP counseling sessions, access to Headspace, backup child, elder care, maternity/paternity leave, pet insurance and so much more!Requirements:* Master's Degree in Social Work (MSW) with a specialization in clinical practice from an accredited school of Social Work.* Meets all state required regulations to practice in the dialysis setting.* Obtained their Clinical License (e.g., LCSW, LICSW), meeting all licensure requirements for their state.* Proficient in all Experienced level Social Worker duties.* Intermediate computer skills.* Demonstrated knowledge of government and private insurance programs.* Excellent interpersonal and communication skillsNow is your time to join Team DaVita. Take the first step and apply now.At DaVita, we strive to be a community first and a company second. We want all teammates to experience DaVita as "a place where I belong." Our goal is to embed belonging into everything we do in our Village, so that it becomes part of who we are. We are proud to be an equal opportunity workplace and comply with state and federal affirmative action requirements. Individuals are recruited, hired, assigned and promoted without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, disability, protected veteran status, or any other protected characteristic.This position will be open for a minimum of three days.For location-specific minimum wage details, see the following link:Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies and experience. DaVita offers a competitive total rewards package, which includes a 401k match, healthcare coverage and a broad range of other benefits. Learn more at **Colorado Residents: Please do not respond to any questions in this initial application that may seek age-identifying information such as age, date of birth, or dates of school attendance or graduation. You may also redact this information from any materials you submit during the application process. You will not be penalized for redacting or removing this information.**DaVita (NYSE: DVA) is a comprehensive kidney care provider focused on transforming care to improve the quality of life for patients globally. The company is a leading provider of kidney care services in the U.S. and has been a leader in clinical quality and innovation for more than 20 years. DaVita is working to help increase equitable access to care for patients at every stage and setting along their kidney health journey—from slowing progression of kidney disease to streamlining the transplant process, from acute hospital care to dialysis at home. As of March 31, 2022, DaVita served 200,800 patients at 2,809 outpatient dialysis centers in the U.S. The company operated an additional 346 outpatient dialysis centers in 11 other countries worldwide. DaVita has reduced hospitalizations, improved mortality and worked collaboratively to help propel the kidney care community to adopt an equitable, high-quality standard of care for patients around the globe.To learn more about what it means to be a part of our Village, visit .DaVita is an equal opportunity employer- Male/Female/Veterans/Disabled. To learn more about what this means click .We maintain a drug-free workplace and perform pre-employment substance abuse testing and background verification checks. We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws.#J-18808-Ljbffr

Emergency Department Nurse jobs in Belgium