- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable ... started? **Main Responsibilities:** **Document Development** + Create high-quality regulatory-compliant clinical documents supporting product life cycle + Ensure timely… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... Database as assigned. + Functions as a PV advisor to Ascendis Clinical Development Organizations, Medical Affairs, Commercial Organizations and PV staff as… more
- Merck (Rahway, NJ)
- …Area: Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of Regulatory ... **Job Description** ** Associate Director , Regulatory Submissions Archive Operations**...and stakeholder feedback. **Required:** Bachelor's degree in a business, scientific , or operational discipline relevant to the life sciences… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director Commercial Regulatory Affairs** **Description** : The role ... of Associate Director of US Commercial Regulatory Affairs...Commercial Regulatory Affairs requires the ability to apply complex scientific and expert regulatory advice and risk assessment for… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director - WW Field Medical & Access Platform Strategy ... + Collaborate with Medical Affairs to align platform capabilities with scientific engagement strategies, ensuring compliance with standards. + Support Access teams… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... regulatory affairs, quality assurance, and other departments to drive scientific excellence, resolve complex technical issues, and ensure compliance with… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial, and public domain information resources to identify relevant… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** We are looking for an experienced Associate Director , Program Manager to join our team. This successful candidate will ... making. **Required Education, Experience and Skills** + Bachelor's degree in a scientific , life science, technical discipline, or relevant field. + Five years of… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …aspirations. Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as the ... team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Product Technical Steward, Cell Therapy Technical Operations ... control and implementation, product comparability and escalated support of technical/ scientific process and analytical issues + Regulatory & Documentation: Provide… more