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Premier Medical Staffing Services is seeking a travel Occupational Therapist for a travel job in Nashville, North Carolina. Autumn Care of Nashvile is a licensed Skilled Nursing Facility (SNF) — a Medicare- and Medicaid-certified nursing home that provides 24/7 medical supervision , not just personal or custodial care. It is part of the Saber Healthcare Group network of senior care communities. Able to accommodate the ever-changing needs of the healthcare landscape, we offer per-diem, contract and direct hire placements to support the unique needs of each industry sector. Premier Medical Staffing Services is Joint Commission Certified, a Military Spouse Employment Partner and is certified as a Women’s Business Enterprise.
The ideal candidate will have a strong background in healthcare administration, regulatory compliance (Medicare Conditions of Participation), clinical coordination, and business operations. Manage all aspects of the agency's clinical and administrative operations, including staff supervision, patient care coordination, budgeting, and resource allocation. Maintain continual survey readiness and lead the agency through state, CMS, and accrediting body inspections (e.g., Joint Commission, CHAP, ACHC). Ensure appropriate supervision and support of clinical staff including RNs, PTs, OTs, SLPs, MSWs, HHAs, and administrative personnel. Comprehensive knowledge of Medicare regulations, OASIS documentation, HIPAA, and CMS guidelines.
Vivo HealthStaff is seeking a highly qualified and motivated MD/JD Attorney who is a previously practicing physician and licensed lawyer to join the Healthcare Practice Group of a nationally recognized law firm. Provide legal counsel on Medicare, Medicaid, and VA/Tricare reimbursement requirements.. Advise clients on fraud and abuse compliance, including structuring transactions consistent with Stark Law, Anti-Kickback Statute, and False Claims Act regulations.. 10+ years of experience advising healthcare clients or engaging in policymaking related to billing and reimbursement including Medicare, Medicaid, and VA/Tricare.. Deep expertise in federal fraud and abuse laws such as Anti-Kickback Statute, Stark Law, and False Claims Act
What You'll Do: Provide standard solo Emergency Room coverage for 12-hour shifts, assessing and treating patients with a variety of acute illnesses and injuries.. Maintain meticulous documentation within the Meditech electronic medical record system.. Current certifications in ACLS, PALS, BLS, and ATLS. Minimum two weeks for credentialing.. NC Medicaid/Medicare credentialing and PECOS enrollment highly preferred.. If you're a qualified and motivated Emergency Medicine physician seeking a locum tenens opportunity to contribute to patient care near Broadway, NC, we encourage you to apply!
We are seeking a dynamic and experienced Director of Nursing (DON) to join our senior leadership team in Roxboro, NC. This newly established role offers a unique opportunity to shape and lead the nursing department in a forward-thinking healthcare setting.. The Director of Nursing will oversee daily nursing operations, ensure delivery of high-quality patient care, and provide strong leadership to the nursing team.. BLS Certification (AHA) – Required upon hire. Master’s Degree in Nursing or Healthcare Administration. Previous experience as a DON or in a nursing leadership role in acute or long-term care settings
Obtain necessary pre and post treatment vital signs and weight and perform vascular access evaluation pre- treatment. Evaluate patients’ vascular access during treatment including arterial and venous monitoring pressures, provide appropriate intervention as needed, document and report any unusual findings to the registered nurse or supervisor.. Ensure collection of lab specimens by appropriate lab courier.. Assists in assuring patient understanding or home dialysis products, benefits of home and how home dialysis can work for them.. Assist in assuring patient understanding of treatment options including demonstration of the peritoneal dialysis set-up.
Reporting and accountable to the Nurse Manager/Director, the Clinical Nurse is responsible for coordinating and delivering patient care utilizing the nursing process in a hospital setting.. Performs bedside point of care testing as required for patient care plan.. Serves as the clinical research nurse of HHT related research studies and participates in all logistical aspects of clinical trials from initial feasibility review to study closeout including CRF creation, budget, subject screening, subject recruiting, data collection as well as development of department standards of practice.. Care Coordination- Providing coordination and support for both the clinical activities and research aspects of the HHT Center, including providing outpatient care, patient assessment, coordination of health care services for the HHT patient population, research coordination, provider and patient education.. Organization Unit: Hemophilia Treatment Center
We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in Brazilian Portuguese and English.. Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits;.. Life science / bio medical background - healthcare related degree (chemistry, biology, biotechnology, pharmacy, nursing).. We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.. PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in Brazilian Portuguese and English.. Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits;. Life science / bio medical background - healthcare related degree (chemistry, biology, biotechnology, pharmacy, nursing). We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
Reporting and accountable to the Nurse Manager/Director, the Clinical Nurse is responsible for coordinating and delivering patient care utilizing the nursing process in a hospital setting.. Performs bedside point of care testing as required for patient care plan.. Serves as the clinical research nurse of HHT related research studies and participates in all logistical aspects of clinical trials from initial feasibility review to study closeout including CRF creation, budget, subject screening, subject recruiting, data collection as well as development of department standards of practice.. Care Coordination- Providing coordination and support for both the clinical activities and research aspects of the HHT Center, including providing outpatient care, patient assessment, coordination of health care services for the HHT patient population, research coordination, provider and patient education.. Organization Unit: Hemophilia Treatment Center
Reporting and accountable to the Nurse Manager/Director, the Clinical Nurse is responsible for coordinating and delivering patient care utilizing the nursing process in a hospital setting.. Performs bedside point of care testing as required for patient care plan.. Serves as the clinical research nurse of HHT related research studies and participates in all logistical aspects of clinical trials from initial feasibility review to study closeout including CRF creation, budget, subject screening, subject recruiting, data collection as well as development of department standards of practice.. Care Coordination- Providing coordination and support for both the clinical activities and research aspects of the HHT Center, including providing outpatient care, patient assessment, coordination of health care services for the HHT patient population, research coordination, provider and patient education.. Organization Unit: Hemophilia Treatment Center
We are one of the largest private duty nursing companies in the nation and growing!. Weekly and/or Daily Pay. Our homecare is always delivered from a place of heartfelt compassion and empathy, and every one of our Registered Nurses (RN)s works together to make sure we achieve outstanding clinical outcomes. Must have and maintain an active, unencumbered license (RN) in the state in which the clinician will practice.. As an employer accepting Medicare and Medicaid funds, employees must comply with all health-related requirements in all relevant jurisdictions, including required vaccinations and testing, subject to exemptions for medical or religious reasons as appropriate.
The Regulatory Affairs Specialist will develop strategies and submissions for projects and issues related to regulatory documents, global submissions, investigations, product development planning, and regulatory agency interaction for the Surgical portfolio.. Assume full responsibility for project submissions, from guidance/strategies/authoring/obtaining approvals, including 510(k) premarket notifications, EU MDD/MDR Technical Files, and/or other documentation required for registration/licensure of products outside the U.S.. 2-3 years of regulatory affairs experience in a regulated environment is required.. Regulatory affairs experience in domestic and international submissions, with 2-3 years of overall class I or II medical devices, is highly preferred.. Basic understanding of, and ability to comply with, business and Regulatory Affairs ethical standards.
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.
Theoria Medical is a comprehensive medical group and technology company dedicated to serving patients across the care continuum with an emphasis on post-acute care and primary care.. Effortless documentation : Conversational and Dragon dictation.. PointClickCare, MatrixCare, and American HealthTech are the most commonly used facility EHR systems. Participating in Theorias Chronic Care Management, Transitional Care, RPM and other medical quality initiatives and programs. Physician must be able to utilize electronic/online medical tools such as EHR systems and state/county medical systems utilized for Death Certificates and administrative functions.
Medical Director- Medicare Fee for Service. The Medical Director is responsible for drafting and developing policies for Medicare fee for service and assisting nurses as needed with review of claims.. Unless expressly allowed by state or federal law, or regulation, must be located in a state or territory of the United States when conducting utilization review or an appeals consideration and cannot be located on a US military base, vessel or any embassy located in or outside of the US.. Medicare fee for service experience strongly preferred.. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.
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)
As Manager, Medical Affairs, you will be responsible for both the clinical and administrative aspects of MMS business.. Minimum: Pharmacy Degree (PharmD) or Bachelors in Nursing (BSN).. PharmD and US pharmacist licensure required OR BSN and US nursing licensure required.. Additional experience within medication or patient safety, quality, regulatory affairs, or medical devices desired.. Knowledge and experience using and interpreting basic biomedical statistical methods is preferred.
We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.. Analyze market data and research insights to identify potential areas for growth and tailor sales strategies accordingly.. Provide regular reports and updates on market intelligence, competitor analysis, and sales performance to the leadership team.. In-depth knowledge of the clinical research industry, including an understanding of CROs, sponsors, and the drug development process.. Strong analytical and problem-solving skills, with the ability to analyze market data and develop actionable insights.
The position will support regulatory intelligence including monitoring regulatory news and updates and summarizing and circulating the same.. Department - Regulatory Affairs. Support on petition filings.. Support regulatory intelligence work involving monitoring updates and news and. Knowledge about Pharmaceutical Product Development.