- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Global Director Medical Affairs (GDMA) Oncology Assets & Pipeline coordinates the development and implementation of the Global Medical ... and assigned Asset Development (Sub-) Teams. In addition, the GDMA leads the Medical Affairs input into the integrated data generation plans spanning outcomes… more
- Merck & Co. (North Wales, PA)
- Job Description Role Summary: The US Regional Director Medical Affairs (RDMA) is responsible for driving execution of scientific & medical affairs ... medical plan for their assigned TAChairs the Regional Medical Affairs Team (RMAT) to ensure execution...in certain states and cities within the United States . Final determinations with respect to… more
- Merck & Co. (Upper Gwynedd, PA)
- …project management skills Preferred Experience and Skills: At least 5 years global or US medical affairs or clinical development experience with proven track ... Job DescriptionThe Executive Director , Global Medical and Scientific Affairs (EDMA) GYN...transmission.Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical Affairs (USOMA). Develops the USOMA strategy and tactical ... as other research areas centered around rare diseases and immune disorders.Summary US Medical Affairs leader for assigned compound under the supervision and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of TA priorities and business needs. Relationships This position may report into the Field Director , Medical Affairs (or in smaller TA's directly into the TA ... SD works closely with the TA Leadership Team and Medical Director team to identify and execute...for scientific resources, communications, and training initiatives for the medical affairs team Serve on Clinical Trial… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … & Public Policy, this position will help lead Daiichi Sankyo's engagement across the United States to ensure patient access to our current portfolio and robust ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… 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 ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… 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 formulation of strategy for global regulatory submissions in Oncology in the US , EU, Japan, China, and other regions. This position ensures alignment of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex- ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… 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 ... development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support across all… 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 ... into the Oncology drug development preferred.Ability to interpret and understand US regulations governing the pharmaceutical industry; general global knowledge of… more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... review and approval of all US promotional materials and serving as the promotional regulatory...as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Diagnostics focused Regulatory Affairs team helps bring new precision medicine advancements to the world by facilitating effective, efficient, and ... strategies and approaches across geographies.Under direction of the Executive Director , Companion Diagnostics/In Vitro Diagnostics, the Principal Scientist/ Director… more
- Merck & Co. (Rahway, NJ)
- …Research & Development, Center for Observational and Real-World Evidence (CORE), Medical Affairs , Policy, Communications and regional and country teams. ... and Product Development Teams (PDTs), (ex. clinical, CORE and medical affairs ), regional and country teams to...in certain states and cities within the United States . Final determinations with respect to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including CCDS and US /EU labeling experience ... pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experienceExperience with ex- US… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Works with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, ... 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)
- …activities that interface with internal and external stakeholders, including Global Marketing, US Medical Affairs , Outcomes Research and key external ... the CMV Pack, a key business driver for the US Pharma Business Unit. The Associate Director ,...marketing strategy through application of the L3 frameworkCollaborate with Medical Affairs to develop and advance scientific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …understand the importance of, key internal constituents - Market Insights, Analytics, Medical Affairs , Sales Training, etc. Present to various internal ... 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)
- …Access and Reimbursement, ORSEA, CRT, Marketing, Integrated Account Management Teams, Medical Affairs , etc.)Primary Responsibilities: Work closely with our ... Job DescriptionThe Associate Director Market Access will work closely with agency...Company's internal functions (promotions management, communications, medical affairs , etc.), brand marketing, etc. and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs , Translational Research, Research, Informatics Services ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...the business functions of Daiichi Sankyo (DS) in the US , EU, Japan, and other global sites. These business… more
