- Merck & Co. (North Wales, PA)
- … Medical directors, as HQ point of contact and Subject Matter Expert for medical review .Serve as product subject matter expert during Global Medical ... thorough understanding of the science behind the medicine and review further unmet medical needs to support...-We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco… more
- Merck & Co. (Rahway, NJ)
- …to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate ... (Word, PowerPoint, Excel, Access). Preferred Experience and Skills Field-based medical experienceClinical research experienceDemonstrated record of scientific/… more
- Tris Pharma (Monmouth Junction, NJ)
- …pricing, distribution, promotion etc.Deep knowledge of the pharmaceutical Legal, Medical , Regulatory review processDemonstrated experience in driving marketing ... team and collaborating with other critical functions including Sales, Managed Markets and Medical teams to help drive the growth of the Tris ADHD portfolio.ESSENTIAL… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …skills, both oral, written and presentation. Demonstrate an ability to perform medical accuracy review with strong attention to detail. Proficiency in ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Media and Omnichannel Orchestration teams on coordination with agencies for Medical /Regulatory/Legal review planning schedules Best Practice Research and ... customer groups. The owner is responsible for coordinating with agencies for regulatory review planning, and ensuring best practices in SEO and SEM. The owner… more
- Merck & Co. (North Wales, PA)
- …may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of clinical data/ ... 5 years of pharmaceutical, clinical drug development, project management, and/or medical field experienceMaster's + 3 years of pharmaceutical, clinical drug… 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
- 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
- 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
- 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
- Novo Nordisk Inc. (Philadelphia, PA)
- …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
- Insmed Incorporated (San Diego, CA)
- …editing [CRISPR, Integrases, etc] base molecular biology techniques.Write and review protocols, SOPs, reports and other product development documentsConceptualize, ... characterize protein performance in vitro.Maintain accurate, detailed, and timely records of analytical procedure development, experimental data, and data… 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
- Novo Nordisk Inc. (Mobile, AL)
- …standing by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records .QualificationsA bachelor's or equivalent degree is ... 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 performance evaluation. This allows the organization to continue advancing medical innovation and improve lives. -Position Description: The main responsibilities ... risk and present results to Senior Management. Perform a review of our Company's top key products in order...-We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco… more
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