- Merck & Co. (Rahway, NJ)
- …for driving the development and execution of the scientific & medical affairs plans in the Value & Implementation organization for the assigned therapeutic area ... position in Our Company Research Laboratories, Global Medical and Scientific Affairs (GMSA). Responsibilities and Primary Activities: Drives development and… more
- Merck & Co. (North Wales, PA)
- …Corporate Affairs and Patient Innovation & Engagement. Support the development and implementation of policies and procedures designed to ensure compliant ... Job DescriptionJob ScopeThe Director, Corporate Affairs and Patient Innovation & Engagement Compliance has global compliance responsibility for all areas of… more
- Genmab (Plainsboro, NJ)
- …support for the overall oncology solid tumor portfolio. The individual will lead the development and execution of the US Medical Affairs strategy that is aligned ... US healthcare market through collaboration with US Commercialization, Global Medical Affairs , Clinical Development , Regulatory, and other cross functional… more
- Merck & Co. (Rahway, NJ)
- …DescriptionThe Executive Director, Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) is accountable for the development and execution of ... skills Preferred Experience and Skills: At least 5 years global or US medical affairs or clinical development experience with proven track record of contribution… more
- Genmab (Plainsboro, NJ)
- …experienced and passionate leader to be a part of our Global Regulatory Affairs (GRA) organization.In this role, the regulatory leader will be primarily responsible ... for the development of global (and US) regulatory strategies (depending on...to the Team Lead of Regulatory Strategy, Global Regulatory Affairs , the key responsibilities include but are not limited… more
- Genmab (Plainsboro, NJ)
- …fulfilling our purpose.The RoleGenmab is looking for an Associate Director, Global Regulatory Affairs , Regulatory Strategy to be a part of our Global Regulatory ... Affairs organization.In this role, you will work in close...the Global Regulatory Lead(s) on a compound in late-stage development to implement the US regulatory strategy for multiple… more
- Merck & Co. (Rahway, NJ)
- …& Controls), you will report to the Director of Device Regulatory Affairs for Autoinjector Development Programs. You will spearhead regulatory activities ... and Drug-Device Combinations (DDDC), ensuring compliance with domestic and international regulations and guidance. This role includes the comprehensive preparation… more
- Genmab (Plainsboro, NJ)
- …Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (eg, Core Data Sheet, ... for the Genmab portfolio of products. This role will be within Global Regulatory Affairs (GRA) and will report to the Sr Director, Labeling, Policy and Intelligence.… more
- Tris Pharma (Monmouth Junction, NJ)
- …and compliance with law, regulations, guidelines and policies Assists VP, Medical Affairs with development of medical strategic and tactical plan; Collaborates ... a leading privately-owned US biopharmaceutical company with a focus on development and commercialization of innovative medicines addressing unmet patient needs. We… more
- Merck & Co. (Rahway, NJ)
- …group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to manage clinical development projects; and assist ... Job DescriptionOur Clinical Development teams manage studies to provide the safety...analysis, regulatory reporting, publication, and presentation at national and international meeting. They will provide internal scientific leadership for… more
- Insmed Incorporated (San Diego, CA)
- …Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility to lead clinical programs across ... different diseases and supervise the clinical development team. This individual will be the primary point person for medical monitoring and oversight of assigned… more
- Genmab (Plainsboro, NJ)
- …and AI to revolutionize our approach to early science, speed up the development of our medicines, and enhance engagement with our customers - the patients ... in the business domains Field Operations, Medical & Regulatory Affairs and US and Japan Market and Commercial Teams...of the role is the active support of product-oriented development (POD) teams in the security of processes related… more
- Tris Pharma (Monmouth Junction, NJ)
- …privately-owned biopharmaceutical company in the US with a focus on development and commercialization of innovative medicines that address unmet patient needs. ... We have more than 150 US and International patents including applications and have marketed several branded and generic products in the US, have licensed our… more
- Merck & Co. (Rahway, NJ)
- …trials. The ideal candidate will be responsible for overseeing the development and maintenance of clinical databases and ensuring the integrity, consistency, ... such as , Clinical Research Associates, Statisticians, Quality Assurance, and Regulatory Affairs to drive data excellence and enhance the efficiency of our clinical… more
- Merck & Co. (Millsboro, DE)
- …(eg safety, compliance)Can work together in multidisciplinary and international teamsPreferred Experience and Skills:Experience in bioprocess development ... BTS-SS team is also responsible for supporting the BTS Process Development (PD) team during new process/product introductions. Within a multidisciplinary environment… more
- Merck & Co. (Rahway, NJ)
- …the Executive Director, Global Pharma Communications is responsible for the development of strategic communications that showcase the strength of the company's ... pipeline, including during late-stage development , distribution and regulatory milestones, in a manner that reflects the company's purpose and upholds its… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with key stakeholders within CSPV and external functions including Clinical Development , Research Development , Regulatory Affairs . Facilitate operational ... around rare diseases and immune disorders. Summary Leads the development and management of DSI's local and global Strategic...Maintains up to date knowledge of local, regional, and international PV regulations. Act as a subject matter expert… more
- International Rescue Committee (New York, NY)
- …PERSON SPECIFICATION Essential Skills, Knowledge, and Qualifications: * Degree in international development / affairs , public administration, social sciences ... ID: req56631 Job Title: Senior Regional Grants and Business Development Coordinator Sector: Grants Employment Category: Regular Employment Type: Full-Time… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …accommodation to individuals with disabilities. **Brief Job Overview** The Policy Analyst, International Government and Regulatory Affairs (IGRA) is an integral ... The candidate will play an active role in the development of evidence-based policy positions to advance USP's mission...individual contributor role that will report to the VP, International Government & Regulatory Affairs . The role… more
- Bristol Myers Squibb (Washington, DC)
- …lives. Read more: careers.bms.com/working-with-us . **Position:** Lead, Global Policy & International Government Affairs , India, Turkey & the Middle East ... Washington, DC **Position Summary** The Lead Global Policy & International Government Affairs , India, Turkey & the...leads across BMS to support affiliate teams in the development of cross-functional annual strategic plans. + Knowledge and… more
