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Core Medical-Perm is seeking a Registered Nurse (RN) Quality Assurance Director for a nursing job in Las Vegas, Nevada. Job Description & Requirements Specialty: Quality Assurance Discipline: RN Start Date: ASAP Duration: Ongoing 40 hours per week Shift: 8 hours Employment Type: Staff DIRECTOR OF QUALITY $90,000-$120,000 We are looking for a healthcare professional who is ready to provide exceptional patient care in this permanent position. Join other healthcare professionals on the annual Club Coremed retreat and you'll see why candidates choose to work with us to expand their careers. We have jobs nationwide in travel nursing, travel allied health, interim, locum tenens, and permanent placements!. Join the staffing agency with Club CoreMed, the best perk in the industry - an all inclusive paid trip to a tropical resort!
Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care. Must be able to demonstrate a working knowledge of laws and regulations governing Medicare, Medicaid and other funding sources. Manages clinical denials, educating referring providers on clinic and payor requirements. Oncology Services Only: Will maintain current Commission on Cancer specific certification in the nurse’s specialty by an accredited certification program or will continue ongoing education by earning 12 cancer-related continuing education nursing contract hours per year or 36 cancer-related continuing education nursing contract hours each accreditation cycle (3 years). As part of our commitment to our patients and employees’ wellness, Parkland Health is a tobacco and smoke-free campus.
Whether your abilities are in direct patient care or one of the many other areas of healthcare administration and support, everyone at Parkland works together to fulfill our mission: the health and well-being of individuals and communities entrusted to our care.. - Must be able to demonstrate a working knowledge of laws and regulations governing Medicare, Medicaid and other funding sources.. Manages clinical denials, educating referring providers on clinic and payor requirements.. Oncology Services Only: Will maintain current Commission on Cancer specific certification in the nurse's specialty by an accredited certification program or will continue ongoing education by earning 12 cancer-related continuing education nursing contract hours per year or 36 cancer-related continuing education nursing contract hours each accreditation cycle (3 years).. As part of our commitment to our patients and employees' wellness, Parkland Health is a tobacco and smoke-free campus.
The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels.. Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees and other support for Scientific Communications. Oversee medical and scientific review of promotional materials for GRC and MRC. Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials. Bachelor's degree a minimum, but M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD preferred.
The Frederick National Laboratory is operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.. Within Leidos Biomedical Research Inc. (operator of the Frederick National Laboratory for Cancer Research), the Clinical Research Directorate (CRD) provides clinical supervision of programs at the clinical end of the research spectrum.. CRD also provides operational support for clinical research and supports clinical trials management, regulation, pharmacovigilance, and protocol development/protocol navigations.. Provides inpatient and outpatient consultative Infectious Disease care for Hematopoietic Stem Cell Transplant (HSCT) Patients. Board certification in Internal Medicine and Allergy and Immunology or Infectious Diseases (other Internal Medicine specialty training will be considered)
Sales Team will be led by Chief Experience Officer with over 20 years of C- level, GM, and Business Development experience in Medical Devices, AI, System Technology and Pharmaceuticals, including 6+ years of entrepreneurship.. Led Quality Assurance and Regulatory affairs activities for 5 new product development and 10 product sustenance programs. Hands on experience in 510K and PMA submissions. Experience in Business strategy, Regulatory, Quality, R&D and Product strategies, managed regulatory concept and quality assurance: feasibility, requirements, usability, integration, testing/automation, verification, reliability, security, validation, post market quality.. Strong team building skills, strategy, and operations thinking, solution & result orientation.
The key functions of this role will be to collaborate with internal and external stakeholders including the Foster City Medical Affairs team, Scientific Publications, Medical Affairs Research, Marketing, Global Commercial Product Strategy, Value and Market Access, Clinical Research, Public Affairs, Government Affairs, Contracts/Finance, Pharmacology, Virology and Legal on both the global and regional levels.. Serve as Medical Affairs therapeutic area expert on Global Publications and Scientific Message Platform committees and other support for Scientific Communications. Oversee medical and scientific review of promotional materials for GRC and MRC. Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials. Bachelor's degree a minimum, but M.D., D.O., PhD (biological or pharmaceutical sciences), or PharmD preferred.
The IT Senior Manager, R&D and Quality Systems is responsible for implementing and supporting R&D and quality business systems required for drug development in the cGMP environment.. This position is responsible for the business analysis, planning, project management, implementation, computer systems validation and ongoing support of business applications in the areas of Research & Development Analytical, Regulatory Affairs, Clinical, Quality Affairs and Quality Control.. Manages the application support of R&D and Quality systems to ensure they meet business needs and user requirements, remains in compliance per cGMP requirements and GAMP5 guidelines.. Experience with R&D, Brand, Quality Assurance / Quality Control, Regulatory Affairs, Clinical, Manufacturing environments regulated by the FDA. Experience with Waters CDS, Trackwise, LIMS, Electronic Regulatory Filing System, Document Management, Quality Systems, Laboratory Operations.
Quality Assurance Analyst supports Data Management development at Rush Health, a clinically integrated network of physicians and hospitals working together to improve health through high-quality, efficient health services covering the spectrum of patient care from wellness, prevention and health promotion, to disease management and complex care management.. Our network includes Rush University Medical Center, Rush Oak Park Hospital, Rush Copley Medical Center, Riverside Medical Center, and over 2000 physician members and 250 non-physician network clinicians.. Provide feedback on data quality (to the RHA Data Sourcing team, as well as to source entities) and regularly evaluate the impact of data quality issues on the end reports and end users.. This will include using master data appropriately in reporting and analytical tool development; documenting master data rules as they relate to reporting needs; working with data stewards to profile and correct master data; and developing user tools to support master data management. QA Tester / Contract To Hire / Hybrid / South Suburbs of Chicago
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 incumbent might also be designated as U.S. Agent (back-up) for the U.S. Office for both ANDAs (GPI USA) and API (GLS India).. Support the U.S. Office for more than 170 approved ANDAs and all unapproved (under review ANDAs) as U.S. Agent back-up for all Glenmark subsidiaries including GPL, GSSA, GPI and GLS. The successful candidate will need to be able to review and sign various submissions to FDA. It will include ANDA cover letter, Form 356H for Original ANDAs, Amendments to ANDAs and/or Supplements to post-approval work.. The email list is provided for such communications which includes Commercial Division Heads, R&D, QA, Legal, Business Development, Project Management, Demand Planning, Marketing and others identified on the list.. Separate communications received from the FDA to support GLS will be sent to the GLS leadership team as identified.. B.S. in Chemistry or Biology, or Engineering degree in Biotechnology or Chemical Engineering
The licensed Clinical Content Developer RN, NP, PA develops and updates the clinical content of Optum Clinical Products.. The Clinical Content Developer is also responsible for quality assurance (QA) of the content and for responding to internal and external client questions and concerns.. We are looking for a licensed RN, NP, or PA, with a broad clinical background who can join our fully remote team and collaborate with us on the development of quality content for the InterQual suite of products.. Collaborate with Product Development (PD), Product Management (PM), Product Owner (PO), and Business Systems Analyst (BSA) as needed. Experience with utilization management (UM), case management, or use of evidence-based guidelines such as InterQual/Clinical Decision Support applications or Medicaid State Policies.
Wellness Programs (Telemedicine, Diabetes Management, Joint & Spine Concierge Care). Education Support & Tuition Assistance (ASN to BSN, BSN to MSN). Keywords: patient care manager RN, hospice RN supervisor, hospice leadership, registered nurse manager, hospice nurse jobs, nurse leader, hospice case management, home health manager, end-of-life care leadership. At Heartland Hospice, part of Gentiva, it is our privilege to offer compassionate care in the comfort of wherever our patients call home.. Our nationwide reach is powered by a family of trusted brands that include: Hospice care: Gentiva Hospice, Emerald Coast Hospice Care, Heartland Hospice, Hospice Plus, New Century Hospice, Regency SouthernCare, SouthernCare Hospice Services, SouthernCare New Beacon
Responsible for increasing membership through direct sales and marketing of Molina Medicare products to dual eligible, Medicare-Medicaid recipients within approved market areas to achieve stated revenue, profitability, and retention goals, while following ethical sales practices and adhering to established policies and procedures.. Develop sales strategies to procure sufficient number of referrals and other self-generated leads to meet sales targets through active participation in community events and targeted community outreach to group associations, community centers, senior centers, senior residences and other potential marketing sites.. Ensure Medicare beneficiaries accurately understand the product choices available to them, the enrollment process (eligibility requirements, Medicare review/approval of their enrollment application, timing of ID card receipt, etc.). 2+ years Medicare, Medicaid, managed care or other health/insurance related sales experience. To all current Molina employees: If you are interested in applying for this position, please apply through the intranet job listing.
As the Associate Director, Clinical Quality Assurance (CQA), you are a key member of the Clinical Quality team maintaining representing Clinical QA in cross functional setting, and advising Cytokinetics Clinical Operations, Biometry and Drug Safety and Pharmacovigilance teams on Clinical Quality matters.. Provide expert CQA advice and strategic mentorship to stakeholders (e.g. Clinical Operations, Data Management, Pharmacovigilance) to support regulatory inspections.. Current and strong working knowledge, interpretation/implementation United States Code of Federal Regulations and European regulations and guidance, including ICH-GCP Guidance requirements governing clinical research conduct and pharmacovigilance operations. Experience with electronic Quality Management Systems and Trial Master File.. Experience in hosting or supporting clinical trial or Drug Safety-related regulatory inspections a plus.
The AIDS Clinical Trial Group ( ACTG ) is a cooperative network funded by the NIH DAIDS to cure HIV and reduce related burdens.. The Executive Director also serves as the chief liaison between UNC and international and multi-institutional clinical trials networks, including ACTG Network, NIH, and other regulatory and funding agencies.. This role requires coordination of a research and clinical trials infrastructure spanning virology, immunology, pharmacology, mycobacteriology, specimen banking, clinical trials design, data management, and regulatory affairs for new drugs and labs.. Excellent interpersonal, verbal and written communication skills to interact with senior hospital leadership, ACTG faculty and staff, collaborating institutions, granting agencies, and vendors.. Expert level knowledge of organizational management theory, financial systems and controls, reimbursement issues, and healthcare regulations; budget management; and alignment of clinical, teaching, and research activities.
Overview Billing Coordinator role at Savant Senior Living.. Skilled Home Health is looking to hire a Billing Coordinator.. Description Skilled Home Health is looking to hire a Billing Coordinator.. Payment Posting: Track and post payments and adjustments accurately to patient accounts.. Knowledge of Medical Billing: Familiarity with medical terminology, healthcare coding, and billing practices
ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.. Lead/moderate DSMB teleconferences, monthly PI and Study Coordinator teleconferences.. Bachelor's degree in biological science with 5+ years of relevant experience in clinical research required. Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks. Exempt Employees are eligible for Unlimited PTO *
UCan do all this and more at UCLA Health.. Experience using online payer sites with the ability to check claim status, denials, and eligibility. Knowledge of CPT, ICD-10, and HCPC codes. UCLA Health is a world-renowned health system with four award-winning hospitals and dozens of primary care practices, specialty practices, urgent care centers and other ancillary locations throughout metro Los Angeles as well as the David Geffen School of Medicine.. If you're looking to experience greater challenge and fulfillment in your career, you can at UCLA Health.
The Clinical and Translational Institute at West Virginia University is currently accepting applications for a (Hybrid) Clinical Research Specialist located in Southern West Virginia.. Participates in the development, coordination, and implementation of research and administrative strategies essential to the successful management of Phase II/III/IV clinical trials research conducted by investigators within the National Institutes of Health (NIH) CARE for HealthTM initiative, which is a pilot to test the feasibility of a network to embed clinical research in primary care settings.. Human subjects protection and related issues - knowledge of professional principles (GCP and IRB guidelines), legal and/or reporting requirements affecting grants and contracts, and adheres to industry and government standards.. Within two (2) years of employment, incumbent must obtain certification as a Research Coordinator through the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA).. From the groundbreaking R1 research at our flagship campus in Morgantown to the career-oriented programs at WVU Potomac State in Keyser, and the technology-intensive programs at WVU Tech in Beckley, the contributions of WVU employees resonate across the state, touching lives and shaping futures.