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Joining DaVita as Patient Care Technician (PCT) is an exciting opportunity to jump start your career in the health care industry!. We also have dedicated training to become a Facility Administrator, and training to become a Regional Operations Director.. To monitor patients before, during and after dialysis treatment including measuring and recording stats, patient observations, and hemodialysis machine setup.. Building long-term relationships with your patients who are suffering from end stage renal disease and are receiving treatment on average 3 times/week.. Health care experience a plus including: BONENT Certified, Certified Hemodialysis Technician (CHT), Certified Nursing Assistant (CNA), Certified Medical Assistant (CMA), or Phlebotomy certification.
Anteris is a science-driven structural heart company that is redefining expectations and advancing the field through cutting-edge solutions focused on restoring native-like physiology versus treating symptoms of structural heart disease.. This role will be responsible for preparing high-quality regulatory submissions, supporting interactions with the FDA and other international regulatory bodies, and ensuring compliance with global requirements related to market authorizations, post-market surveillance, and regulatory reporting.. Ensure Regulatory Affairs participation on cross-functional project teams supporting new product development and product modifications.. Author, review, and approve internal procedures related to regulatory affairs operations and compliance.. Hands-on leadership of regulatory submissions for Class III/PMA devices, including FDA (IDE, PMA) and EU (MDR, CA, CE Mark) pathways.
Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.. At every stage, Veranex clients realize efficiencies in cost and time, while our comprehensive solutions unify the entire development process.. Veranex partners with the world's most influential life science and medical device companies to research, design, develop and commercialize new healthcare technologies and treatments to advance patient care.. The Vice President of Program Management provides organizational leadership and is responsible for leading the Product Design and Engineering Program Management organization.. Responsible for deploying a Program Management team to achieve program goals and effectively balance the competing priorities of: Client Success, Technical Success, Team success
Clinical trials advance our clinical services, bringing the very newest insights in patient care. This position will be working 24 hours every two weeks on the day shift, 8 hour shifts and every other weekend. Six months of recent direct care experience in a long term, home care or acute care setting. Appropriate roles may include, Nursing Assistant, PCA, Resident Assistant or Emergency Room Technician)OR. Current enrollment in an LPN, RN or Nurse Practitioner program, and completion of one (1) semester of clinical rotation within the program
Become a Certified Nursing Assistant (CNA) at Redeemer Health & Rehab Center today.. Our all-inclusive training program is designed to prepare you for success: CNA Training Program: 75 hours, with a blend of online and in-person learning.. About Us: Redeemer Health & Rehab Center is a Medicare/Medicaid-certified facility offering 24-hour skilled nursing care, on-site rehabilitation, and restorative nursing programs.. As part of Cassia, an affiliation of Augustana Care and Elim Care, we are a Christian mission organization with over 200 years of combined experience.. At Redeemer Health & Rehab Center, you're not just starting a job; you're joining a caring community committed to excellence and support.
Certified Registered Nurse Anesthetist. We are seeking a skilled and compassionate Certified Registered Nurse Anesthetist (CRNA) to join our healthcare team at a leading medical facility in Ohio. As a CRNA, you will be responsible for delivering anesthesia care to patients undergoing various medical procedures, ensuring safety, comfort, and optimal outcomes throughout the perioperative process.. This is an excellent opportunity for an experienced CRNA to contribute to patient care in a supportive and dynamic environment.. Valid RN license in Ohio and certification as a CRNA by the National Board of Certification and Recertification for Nurse Anesthetists (NBCRNA).. Strong knowledge of anesthesia techniques, pharmacology, and patient care protocols.
Certified Nursing Assistant (CNA) , Dementia Screening Support - Minneapolis, MN. Kelly Science & Clinical is seeking reliable and professional Certified Nursing Assistants (CNAs) or Certified Medical Assistants (CMAs) to support a dementia screening program in nursing home settings. This non-clinical role focuses on administering a single component of the Creyos Dementia Screening Tool. It's an excellent opportunity for CNA/CMAs looking for a low-stress, meaningful position that doesn't involve direct patient care tasks. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. It's the ripple effect that changes and improves everything for your family, your community, and the world.
As a Field Medical Director, MSK Surgery you will be a key member of the utilization management team.. Utilizes medical/clinical review guidelines and parameters to assure consistency in the MD review process to reflect appropriate utilization and compliance with SBU`s policies/procedures, as well as Utilization Review Accreditation Commission (URAC) and National Committee for Quality Assurance (NCQA) guidelines.. May assist the Senior Medical Director in research activities/questions related to the Utilization Management process, interpretation, guidelines and/or system support.. Participates in on-going training per inter-rater reliability process.. Not under current exclusion or sanction by any state or federal health care program, including Medicare or Medicaid, and is not identified as an "excluded person" by the Office of Inspector General of the Department of Health and Human Services or the General Service Administration (GSA), or reprimanded or sanctioned by Medicare.
Medical Director - Endocrinology (Obesity). A growing biotech with an expanding late-phase pipeline is seeking an experienced Medical Director to lead clinical development efforts in endocrinology, with a focus on obesity.. Contribute to and execute the Clinical Development Plan for obesity programs. Partner with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, and Medical Affairs. MD (Board Certification or PhD in Endocrinology or related field preferred)
The Regulatory Affairs Specialist plays a key role in supporting the registration and compliance of pesticide products across state and federal agencies.. Manage all state pesticide product registrations , including new applications, renewals, label amendments, and sales reporting.. Assist in interpreting and applying state, federal, and international pesticide laws and regulations.. Experience: 2+ years in Regulatory Affairs, Compliance, or a technical field (preferred).. Operates effectively within EOS, embracing clarity, accountability, and structured problem-solving
Pelvic Health (PH)therapies treat patients suffering from overactive bladder, non-obstructive urinary retention and fecal incontinencewith our sacral neuromodulation (SNM) systems InterStim X and InterStim Micro; and our percutaneous tibial neuromodulation (PTNM) system NURO. PH is part of the Neuroscience portfolio.. Partner with Integrated Business Planning (IBP) teams to ensure lifecycle inputs are embedded in short- and long-term planning processes.. Create and maintain operational processes that embed lifecycle management at both the inception and conclusion of the NPI process, ensuring long-term product viability is considered at every stage.. 5 years of experience in Instrument Engineering, Healthcare IT, Clinical Research, Regulatory Affairs, Marketing, Operations, or Quality.. Proficiency with enterprise business systems such as SAP, JD Edwards, and Product Data Management tools (e.g., Enovia, MRCS, Agile).
Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.. This Regulatory Affairs Project Manager position is an onsite opportunity working out of our St. Paul, MN location in the Abbott Vascular Division.. As an individual contributor, the function of a Regulatory Affairs Project Manager is to combine knowledge of scientific, regulatory, and business issues to enable products that are developed, manufactured or distributed to meet required legislation.. Advanced degree or additional professional training in regulatory affairs (RA) desired.. Previous experience with PMA / IDE submissions
The Research Nurse II is responsible for providing nursing technical expertise and overall execution of clinical trials, with an emphasis on later phase (II-III) clinical trials and an introduction to phase I trials.. The incumbent will be expected to follow Good Clinical Practice (GCP) and all organizational policies and procedures for patient safety and data integrity, including but not limited to the Institutional Review Board (IRB), Food & Drug Administration (FDA), Code of Federal Regulations (CFR), and International Conference on Harmonization (ICH) guidelines.. Utilizes nursing education to contribute to study start-up activities, including site initiation visits, protocol review of feasibility and suggestions for revision, study and clinical staff training.. The Masonic Cancer Center (MCC) is an NCI-designated Comprehensive Cancer Center dedicated to cancer research, education, and patient care for the citizens of Minnesota and the surrounding region.. At the University of Minnesota, we are proud to be recognized by the Star Tribune as a Top Workplace for 2021, as well as by Forbes as Best Employers for Women and one of America's Best Employers (2015, 2018, 2019, 2023), Best Employer for Diversity (2019, 2020), Best Employer for New Grads (2018, 2019), and Best Employer by State (2019, 2022).
The Regulatory Affairs Manager is responsible for leading regulatory functions and serves as management representative. Oversee, supervise, and provide direction in the following areas: Regulatory Strategy, Product Registration and Market Clearance, Device History Record Review, Employee Training, Design History File Maintenance, and Labeling. Assess the impact of changes on current clinical investigations and FDA filings. Bachelor's Degree or equivalent is required; Minimum of 10 years progressively responsible experience in the medical device industry is required; Minimum of 7 years within quality systems and/or regulatory compliance functions is required. This position is subject up to travel up to 15% of the time to include both domestic and international travel.
Join Novartis as a Medical Science Liaison (MSL) in a field-based, customer-facing, non-promotional medical and scientific role, where you will inform and shape medical strategy through the application of a curious mindset to collect impactful and actionable insights.. Collaborate with internal colleagues (e.g., HEOR, access, marketing, commercial, sales) within the assigned therapeutic area and territory to advance clinical practice while maintaining customer centricity and a One Novartis approach in accordance with Novartis compliance standards.. Education: Graduate degree in science or healthcare required; doctoral degree preferred (MD, PhD, DNP, PharmD, etc.. Medical Science Liaison (MSL), Medical Affairs - North Central. Principal Medical Writer (Contract-to-Hire)Senior Medical Writer (Contract-to-Hire)Sr. Program Manager, Medical Affairs (Heathcare Systems Partnerships)Director of Regulatory Affairs - Medical Devices
Coordinates, compiles, and submits US regulatory filings for new and modified products, including PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, PMA & IDE Annual Reports. Demonstrated experience authoring/supporting a variety of regulatory submissions for US and EU, such as original PMAs, PMA Supplements, pre-submissions, IDEs, 510(k)s, and MDR Technical Documentation. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).. Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).. Job Segment: Regulatory Affairs, Medical Device, Compliance, Clinical Research, Medical Research, Legal, Healthcare
Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.. This Regulatory Affairs Project Manager position is an onsite opportunity working out of our St. Paul, MN location in the Abbott Vascular Division.. As an individual contributor, the function of a Regulatory Affairs Project Manager is to combine knowledge of scientific, regulatory, and business issues to enable products that are developed, manufactured or distributed to meet required legislation.. Advanced degree or additional professional training in regulatory affairs (RA) desired.. Previous experience with PMA / IDE submissions
The Vice President, Compliance Business Partner is a key leader on the Compliance team and serves as the main point of contact between the Compliance team and the business teams, including the Commercial, Purchasing and Business Development, Revenue Cycle Management, Ambulatory Infusion Center, Naven Health and acquired business teams.. Serves as a subject matter expert in health care compliance including, but not limited to FWA, Medicare & Medicaid billing requirements, and interactions with healthcare professionals.. Collaborate with Compliance Operations on healthcare professional engagement process, Corporate Integrity Agreement requirements, internal investigations, policy updates, exceptions approval, training , monitoring and auditing activities, and implementation of corrective actions.. Proven experience in a leadership role of a compliance function in the healthcare industry, with a deep understanding of healthcare regulations, such as the Anti-Kickback Statute, Stark Law, HIPAA and Medicare/Medicaid requirements.. Juris Doctor (JD) degree from an accredited law school.
Medical Science Liaison (MSL), Medical Affairs - North Central Join to apply for the Medical Science Liaison (MSL), Medical Affairs - North Central role at Madrigal Pharmaceuticals. Advanced degree in healthcare or science-related area of study (e.g., MD/DO, PharmD, PhD, DNP, PC) or other life sciences or equivalent with solid medical/technical background.. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.. Senior Medical Writer (Contract-to-Hire) Principal Medical Writer (Contract-to-Hire) Sr. Program Manager, Medical Affairs (Heathcare Systems Partnerships) Director of Regulatory Affairs - Medical Devices Minneapolis, MN $185,000.00-$225,000.00 1 week ago. Medical Science Liaison, Rheumatology - CO, MN, OK, NE, SD, & ND Minneapolis, MN $115,000.00-$197,850.00 1 week ago
The Case Management program aims to serve our members with the highest needs to navigate the healthcare system.. This Case Management opportunity will serve our North Dakota Medicare Advantage Dual Special Needs Plans (DSNP) membership.. Engaging the member/caregiver in an annual Health Risk Assessment (HRA) as required by CMS. Care plan collaboration and development based on individual needs identified in the HRA, including the member, family/caregiver and provider care team. Certified Case Manager (CCM) preferred, or ability to obtain within two years of hire