- Legend Biotech USA, Inc. (Raritan, NJ)
- …Document Control Specialists to meet goals and deadlines.Serve as a Document Control reviewer for new and revised procedures and documents to ensure compliance with ... workflow handling and electronic system usage, as needed.Manage the periodic review process for procedures, as needed.Issue batch related documentation and labels… more
- Merck & Co. (Rahway, NJ)
- … medical affairs or clinical development experience with proven track record of contribution to medical or clinical development strategiesCustomer expertise, ... Job DescriptionThe Executive Director, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) is accountable for the development and execution of… more
- Genmab (Plainsboro, NJ)
- …conduct of clinical trials in oncology. Proficiency in clinical data review and interpretation.Solid experience in translating medical /clinical information into ... and authentic is essential to fulfilling our purpose.The Role The Director of US Medical Affairs Solid Tumors Strategy will report to the Senior Director, US … more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary The Hematology US Scientific Director, Medical Affairs (SDMA) is a regionally based position in our Company's Research Laboratories, US ... Medical Affairs. The role drives scientific excellence and optimizes...(AOI) consultation and dissemination, MISP data highlights/updates/training, and scientific review aligned with incumbent expertiseRequired Qualifications, Skills, & Experience… more
- Merck & Co. (St. Louis, MO)
- Job DescriptionRole SummaryThe Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... bidirectional exchange of scientific or medical information with Scientific Leaders (SLs). The role provides balanced, factual, scientific information about… more
- Taiho Oncology (Philadelphia, PA)
- Medical Science Liaison Philadelphia, PA, USA Virtual Req #411 Thursday, November 21, 2024 Looking for a chance to make a real difference in the oncology space? ... join us. Territory Coverage: PA, Upstate NY, DC, MD, DE Position Summary: The Medical Science Liaison (MSL) is a field-facing representative of the Medical … more
- Novo Nordisk Inc. (Houston, TX)
- …standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records . Qualifications Bachelor's or equivalent degree, ... I maintains relationships with physicians, physician assistants, nurse practitioners, medical assistants, pharmacists, nurses and other paramedical customers and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …regulations.Key Responsibilities Manage the team responsible for drug product batch record review and drug product release practices.Develop positive ... and improvement of QA practices to ensure accurate documentation of all review and release activities for drug products, including manual and electronic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and maintenance of the CCDS, US and EU labeling, and manages the review of country labeling deviations for assigned Daiichi Sankyo products ensuring compliance with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for budget records and prepares documents required for the budget review processes Develops requests for proposals; evaluates and provides input into vendor ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...pertinent factors based on the project; and coordinates legal review of finalized contract; Manages vendors to ensure the… more
- Merck & Co. (Durham, NC)
- …inspections, presenting on topics as needed. Executes and manages Operations batch record review within established timelines for release and effectively ... Science (BS) degree in Engineering (such as Chemical, Mechanical, Bio-Engineering, Bio- Medical Engineering, Industrial Engineering, etc.) or Science Fields (such as… more
- Novo Nordisk Inc. (West Hollywood, CA)
- …standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records . Qualifications Bachelor's or equivalent degree, ... of obesity, yet only 2% of them receive dedicated medical treatment. By joining the Obesity Commercial team, you...backed by Novo Nordisk's long term commitment and track record in helping people living with chronic disease achieve… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and maintenance of the CCDS, US and EU labeling, and manages the review of country labeling deviations for assigned Daiichi Sankyo products ensuring compliance with… more
- Aequor (Salt Lake City, UT)
- …low complexity issues on the manufacturing/packaging floor and during batch record documentation/ review . 6. Investigations and Recommendations: Participate in ... issues that occur on the manufacturing/ packaging floor and/or during batch record documentation/ review and providing directions for situations of low… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our success is backed by ethical integrity, forward momentum, and ... and budget management as necessary. The candidate will also have a proven track record of developing talent from a diverse scientific background and will have the… more
- Merck & Co. (Rahway, NJ)
- …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... development activities including engineering design, engineering analysis and testing, medical device design controls, risk management, test method/fixture development,… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Medical Writing & Disclosure (MW&D) Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical ... integrate health literacy/equity and SDoH into organizational practicesServe on the Review Committee for Patient Engagement, Diversity & Health Literacy Investigator… more
- Merck & Co. (North Wales, PA)
- …Sr. GTOS should possess a Bachelor or Master of Science degree in medical /pharmaceutical/biological sciences with at least 5 years of career experience including 3-5 ... Desired skills include formal education and or training in medical , marketing, and/or communication. An ability to analyze clinical...with support from GO TA lead, at cross functional review meetings such as LDRC/EDRC TA DRC, FORce, Operational… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Regulatory Intelligence (PVRI) and dissemination across CSPV stakeholders. Participates in the review and management of monthly, quarterly, and ad hoc PVRI reports… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... CCDS; Ensures implementation of CCDS/labeling agreements with licensing partners.Conduct Label Review Committee Meetings: Prepares documents for review by… more
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