- Daiichi Sankyo, Inc. (Bernards, NJ)
- …reviewer comments/requestsoPublication tracking and announcement, in coordination with Medical Information Education (ME)- Support global medical ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Merck & Co. (North Wales, PA)
- …Teams, Franchise Teams, Regional Product Directors, affiliates, Public Affairs, and Medical Education to ensure value evidence programs are consistent with marketing ... to document the burden and cost of diseases, unmet medical need, patient reported outcomes (PRO) and the value...the team.- Present research plans and results to internal review and governance committees; to external experts and agencies… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records . Development Of People Supervisory. Ensure that ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk...experience in therapeutic area (Hemostasis) is preferred Proven track record of success, especially in establishing relationships with opinion… more
- Merck & Co. (Rahway, NJ)
- … medical affairs or clinical development experience with proven track record of contribution to medical or clinical development strategiesCustomer expertise, ... DescriptionThe Executive Director Pulmonary Hypertension, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) (referred to as EDMA) is… more
- Eisai, Inc (Nutley, NJ)
- …study. Maintain Process Guides and other resources. Continue partnership with the Medical Affairs Professional Society (MAPS) Maintain training records . Conduct ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...MSL managers. Develop congress abstract tracker, assign MSL coverage, review MSL reporting responsibilities, collate and distribute Congress Report,… more
- Merck & Co. (South San Francisco, CA)
- …to therapeutic area governance, functional area experts and development review committees.Contribute to assessment of internal and external opportunities identified ... 25%Qualifications, Skills & Experience Education: MD or MD/PhD Required: Proven track record in clinical medicine or clinical research, and background in biomedical… more
- Merck & Co. (Rahway, NJ)
- …are manufactured in compliance with cGMP and regulatory filings. Perform independent quality review and approval of batch records , testing data, and related ... Global Development Quality Operations - API, is responsible for independent review and approval of documentation to support Good Manufacturing Practice (GMP)… more
- Taiho Oncology (FL)
- …you to join us. Territory Coverage: FL, GA, MS, PR, AL Formally known as Medical Science Liaison Position Summary: The Sr. Manager, Medical Field is a ... disease states, and facilitation of clinical research. The Sr. Manager, Medical Field integrates clinical/scientific expertise and knowledge to ensure successful… more
- Merck & Co. (South San Francisco, CA)
- …populations.We are seeking a highly qualified physician-scientist with a proven track record in the pharmaceutical industry as well as independent academic research ... to therapeutic area governance, functional area experts and development review committees.Contribute to assessment of internal and external opportunities identified… more
- Eisai, Inc (Raleigh, NC)
- …across applicable quality assurance functions in a GMP setting (eg, batch record review , SOP writing, auditing, batch release functions, deviation investigation ... effective collaboration across teams.ResponsibilitiesExecute core processes within Quality area: Review manufacturing batch records for completeness, accuracy,… more
- Novo Nordisk Inc. (Dayton, OH)
- …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
- Merck & Co. (Rahway, NJ)
- …and knowledge of product and process development in the (bio)pharmaceutical and medical device industries to set tactical and strategic direction on programs to ... launch. The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, verification, validation… more
- Merck & Co. (Rahway, NJ)
- …Job descriptionThis position will be responsible for leading and implementing medical device and combination product design controls for both new products ... the preparation of materials for program presentations for management review and regulatory submission.Contribute to the development, implementation, and continuous… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... 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
- AUROBINDO (Durham, NC)
- …etc.HR database management which includes data entry, maintaining accurate record keeping and producing reports, as needed. (currently utilizing Paylocity ... resumes, conducting phone screens, and interviewing.Assist with benefits administration including medical , dental, vision, COBRA and 401(k), health and welfare open… more
- Merck & Co. (Upper Gwynedd, PA)
- …of potential risks.Lead the development, communication, lifecycle management and review of the CMC Regulatory Strategy Document for assigned projects.Provide ... regulatory leadership as needed in product in-license/due diligence review and product transition to the Post-Approval Pharm CMC team.Manage execution of CMC… more
- Novo Nordisk Inc. (Walnut Creek, CA)
- …standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records . Qualifications Bachelor's or equivalent degree, ... other field-based employees (eg, DBMs, DCSs, Market Access Team, Diabetes Educators, Medical Liaisons) covering the same geographic areas. The Specialty Field Sales… more
- Merck & Co. (Rahway, NJ)
- …are maintained and are suitable for both GMP and developmental use.- Author, review and approve GMP procedures and documentation, with an emphasis on Qualification ... -Maintenance & Engineering techniques and management and Capital Project management.-Track- record of independent problem-solvingSAP Training and skills - Project… more
- Merck & Co. (Rahway, NJ)
- …11 ComplianceSupport standardization activities for System Development Life CyclePrepare, review , and approve documentation such as master inventory lists, ... both independently and cross-functionally to deliver on complex objectives-Proven track record of strong technical and innovative problem solvingDesire and ability… more
- Merck & Co. (Millsboro, DE)
- …summaries (ISS), outlines of production and special outlines). Alternatively, may review and prepare registration documents for export markets.May serve as point ... lead in creation of GRA standard international dossiers for US Biologicals.May review market advertising and promotions (A&P) for US Biologicals in compliance with… more
