- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… 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 ... and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Marketing, Medical Affairs, Regulatory Affairs, Supply Chain Technical Operations , Pharmaceutical Technology and others where applicable. Identifies areas ... Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... rare diseases and immune disorders. SummaryThis position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT)… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... research areas centered around rare diseases and immune disorders.Job Summary: The Director , Diagnostic Sciences will be responsible for end-to-end process for CDx… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Japan, and other global sites. These business functions include: Clinical Operations , Clinical Development, Biostatistics and Data Management, Regulatory ... 7 years experience in applications development and operation in the pharmaceutical industry within the appropriate regulatory guidelines.7+ years' experience… more
- Merck & Co. (Rahway, NJ)
- …and partnering for Pharmaceutical development/ CMC with Quality, Regulatory , Operations , Non-clinical, Clinical, and other functional areasExperience with ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Tris Pharma (Monmouth Junction, NJ)
- …Assurance provides strategic leadership and direction for Clinical Quality Assurance Operations , ensuring compliance with regulatory standards and driving ... Junction, New Jersey, Tris has an immediate opening for a full-time permanent Director /Senior Director , Clinical Quality Assurance. This is a hybrid position.… more
- Merck & Co. (Rahway, NJ)
- …of increasing responsibility and independence in a similar role in pharmaceutical drug development, regulatory agency, or academia.Educational background in ... Point, PA / Rahway, NJ is seeking a curious and collaborative Director to support our rapidly expanding cardiology respiratory, metabolism and ophthalmology… more
- Merck & Co. (Rahway, NJ)
- …trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the ... clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direcUindirect team members through proactive… more
- Merck & Co. (Rahway, NJ)
- …Jersey and reports to the Executive Director of FLEx Non-Sterile Operations in Pharmaceutical Operations & Clinical Supply.- Primary Responsibilities: ... Close partnership with colleagues from Formulation Sciences, Device Development, Quality, Regulatory Affairs, Engineering, and Analytical will be required to ensure… more
- Merck & Co. (Rahway, NJ)
- …and partnering for Pharmaceutical development/ CMC with Quality, Regulatory , Operations , Non-clinical, Clinical, and other functional areasExperience with ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other functional areas such as biostatistics, data management, clinical operations , pharmacovigilance, regulatory affairs, etc. Qualifications: Successful ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...and figures (TLFs) needed for clinical study reports and regulatory submissions, as well as in-house validation of this… more
- Merck & Co. (Washington, DC)
- …to provide their expertise in policy advocacy and for managing its day-to-day operations .The Associate Director will also independently review the Public Policy ... Job DescriptionPosition Description: Associate Director , Policy Advocacy The Associate Director , Policy Advocacy serves as the senior expert in the Global Public… more
- Merck & Co. (Washington, DC)
- …think tanks or business associations responsible for healthcare, commercial trade, regulatory , or intellectual property- Pharmaceutical sector, medical device, or ... Job DescriptionPosition Description: Director , Policy Development The Director , Policy...on above product policy issues-Ability to master complex policy, regulatory and legislative issues, think creatively and rapidly develop… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Japan, and other global sites. These business functions include: Clinical Operations , Clinical Development, Biostatistics and Data Management, Regulatory ... More Years experience in applications development and operation in the pharmaceutical industry within the appropriate regulatory guidelines. requiredExperience… more
- Merck & Co. (Washington, DC)
- …think tanks, or business associations responsible for healthcare, commercial trade, regulatory , or intellectual property Pharmaceutical sector, medical device, ... Job DescriptionPosition Description: Associate Director , Policy Strategy and Capabilities The Associate ...your employment may pose an undue burden to business operations , in which case you may not be offered… more
- Merck & Co. (North Wales, PA)
- …Leaders; and ensure all Scientific Leader engagement activities comply with regulatory , legal, and ethical standardsCommercial lead in driving engaging presence of ... of progressive experience across marketing or related experiences in pharmaceutical (ie medical affairs) or biotechnology industriesDemonstrated ability to develop… more
- Merck & Co. (North Wales, PA)
- …currently recruiting for someone to join our US marketing team as the Associate Director , Product Marketing Owner - HCC / Ecosystem for the HIV Franchise. -Ideal ... ownership of brand and HCC strategy and execution. This position will report to the Director , US Commercial Leader (USCL) and will be based in the Upper Gwynedd, PA… more
- Tris Pharma (Monmouth Junction, NJ)
- …between marketing and other cross-functional teams (ie, Medical Affairs, Sales, Regulatory Affairs, Operations , etc.)Collaborates closely with Analytics team to ... with advocacy organizations and Key Opinion Leaders (KOLs)Strong understanding of pharmaceutical marketing practices including the regulatory environment and… more
