- Daiichi Sankyo, Inc. (Bernards, NJ)
- …industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience with ex-US labeling ... (outside the US) preferred Travel - Ability to travel up to 10%Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years in the pharmaceutical industry preferred1 or More Years in regulatory affairs requiredExperience in (s)NDA/BLA filing to FDA preferred Travel Ability to travel ... up to 20%. In-house office position that may require occasional travel (global). Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity,… more
- Merck & Co. (North Wales, PA)
- …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 expert with marketing, legal, and medical teams to ensure that promotional practices are consistent with regulatory guidelines, our company's policies, and support business objectives.Serve as the… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Executive Director, Global Medical and Scientific Affairs (EDMA) GYN Malignancies is accountable for the development and execution of scientific & ... medical affairs Value and Implementation (V&I) plans for their assigned...team of TA dedicated global and regional directors and associate directors. The EDMA engages with global scientific leaders… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director, Global Medical Affairs (GMA) Oncology- Medical Content ... is responsible for execution of global scientific and training deliverables. The Associate Director develops and executes Medical Content and Training plans and… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Director Market Access for a prescription medicine , will work closely with agency partners, internal brand colleagues, promotions, ... This role will report to the Director, Oncology Market Access.The Associate Director will be responsible for supporting tactical execution and development… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, Global Oncology Communications , will support the creation and implementation of external communications strategies, plans and ... pipeline, in partnership with key stakeholders and our Corporate Affairs and Enterprise strategy.Lead and support late-stage oncology pipeline communications… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions ... healthcare providers, key stakeholders and policymakers. Our Market Access and Public Affairs professionals ensure that the latest therapies and products reach the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, Pharmaceutical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and term libraries. Provides support for other projects within Legal and Corporate Affairs including coordinating and drafting agenda for Legal Affairs Meetings ... accommodation. Education Qualifications (from an accredited college or university)- Associate 's Degree required- Bachelor's Degree preferred Experience Qualifications- 4… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department Novo Nordisk's Market Access and Public Affairs team engages diverse stakeholders across political and healthcare landscapes to forge solutions ... healthcare providers, key stakeholders and policymakers. Our Market Access and Public Affairs professionals ensure that the latest therapies and products reach the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs , Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, ... Regulatory/Risk Management, Quality Assurance, Medical Affairs , Translational Research, Research, Informatics Services, Project Management and Operational… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary: The Associate Director, Regional Marketing Conventions & Field Programs will be ... and more, while ensuring adherence to DS policies and procedures. The Associate Director, Regional Marketing Conventions & Field Programs is responsible for managing… more
- Merck & Co. (Washington, DC)
- Job DescriptionPosition Description: Associate Director, Policy Strategy and Capabilities The Associate Director, Policy Strategy and Capabilities is ... team, reporting to the Executive Director, Policy Development & Strategy.The Associate Director will develop and maintain the strategic planning digital platform,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical ... Affairs ' externally sponsored clinical research (ESR) initiatives, ensuring strict adherence to Good Clinical Practices (GCPs), relevant Standard Operating… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed ... drugs for oncology indications. The Associate Vice President will manage and oversee the entire cycle of clinical development, including study design, initiation,… more
- Merck & Co. (Rahway, NJ)
- …part of our company's Social Business Innovation (SBI) department within Corporate Affairs . The ESG team works cross-functionally with senior leaders and partners in ... sustainable and healthy future for people and communities everywhere.The role of Associate Director, ESG Strategic Reporting is a unique opportunity to join our… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure successful implementation of CDx and data collectionSupports Regulatory affairs in providing content and providing review of documents supporting CDx ... submissions to the FDA and other health authorities globallyFor late-stage programs, executes the Diagnostic development strategy for a project under the direction of the GPT CDx representative while keeping abreast of regulatory and policy updates in the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA ... team and serves as ad hoc member to the Global Project Team for late stage projects. This position manages multiple biological developmental projects with supervision, including working with contract manufacturing organizations CMO. This position develops… more
- Daiichi Sankyo, Inc. (Nashville, TN)
- …seeking a Medical Science Liaison (MSL) to join the Field Medical Affairs Team. The MSL develops ongoing professional relationships with national and regional ... related products developed and commercialized by DSI. This is a US Medical Affairs , Field based role. This territory currently covers the following states: NC, SC,… more
