- Bristol Myers Squibb (Devens, MA)
- …their personal lives. Read more: careers.bms.com/working-with-us . The **Associate Director , Product Technical Steward, Cell Therapy Technical Operations (CTTO)** is ... escalated support of technical/scientific process and analytical issues + Regulatory & Documentation : Provide technical content for documents such as PPQ protocol or… more
- Bristol Myers Squibb (New York, NY)
- …lives. Read more: careers.bms.com/working-with-us . **Position summary** The Associate Tax Director , Tax Counsel provides tax strategy, planning, and execution on a ... policies and strategies to comply with transfer pricing regulations and documentation requirements. **Required Skills:** + JD, bachelor's degree in accounting or… more
- Akumin (TN)
- We are seeking an experienced, strategic, and results-driven Senior Director of Billing and Collections to lead our end-to-end billing operations. This senior ... Foster cross-functional collaboration with finance, IT, compliance, operations, and clinical leaders to ensure seamless revenue cycle integration. **Billing… more
- Fresenius Medical Center (New York, NY)
- …legal, compliance and regulatory requirements and programs. Collaborates with the Medical Director and the Clinical Coordinator /Charge Nurse or Nurse Supervisor ... to and implemented by the facility staff. + Maintains integrity of medical records and other FMS administrative and... Coordinator /Charge RN or Nurse Supervisor and Medical Director to optimize clinical staffing. + Provides… more
- Bristol Myers Squibb (Princeton, NJ)
- …+ Support the creation and maintenance of technical specifications, process documentation , and SOX/audit compliance artifacts. + Conduct solution reviews, validate ... and analytics tools to extract insights from large datasets, ensuring the accuracy and integrity of Model N data for analytical and reporting purposes. + Mentor and… more
- Merck (Rahway, NJ)
- …and execute design verification strategies that successfully supports the clinical instruction(s) and commercial market approval(s) of combination products. ... strategies for assigned drug-device combination product program(s) for successful clinical introduction(s) and commercial market(s) approval(s). + Define design… more
- AbbVie (North Chicago, IL)
- …and help drive first pass approvals. Responsibilities + Author and coordinate submission documentation for all phases of clinical development of biologics, with ... ensuring that the CMC submission strategy is aligned closely with the clinical /regulatory development strategy and provides drug development experience and advice to… more
- AbbVie (Mettawa, IL)
- …executing statistical components of plans for research studies that prove the clinical , economic and humanistic value of pharmaceutical assets. Position uses sound ... theories, methods, and applies technical programming skills and experience to analyze clinical , survey and claims databases. Role supports the department as a… more
- University of Utah (Salt Lake City, UT)
- …Director . 2. Supervise graduate students in developing and completing required clinical documentation (ie, chart notes, diagnostic reports, patient data ... in the Speech-Language-Hearing Clinic and contracted off-campus facilities as assigned by the Director of Clinical Education - Audiology, with approval by the… more
- Bristol Myers Squibb (Summit, NJ)
- …to support process data trending programs for the commercial and late stage clinical products across the cell therapy network. This individual will be responsible ... site data, trending to enable root cause analysis, CAPA identification, and documentation . + Serve as the interface between sites, product teams and laboratories… more
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