- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …in the relevant therapeutic area. + Minimum of 7 years of experience in Medical Affairs or Scientific Communications within the pharmaceutical or ... The Associate Director , Scientific Communications manages the execution...policies and external regulatory requirements. + Collaborate cross-functionally with Medical Affairs , Clinical Development, Regulatory, Legal, and… more
- Takeda Pharmaceuticals (Boston, MA)
- …in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly complex or multiple ... approvals of project(s) of responsibility or oversees direct reports responsible. The Director will lead all submission types. + Accountable for building global… more
- Veterans Affairs, Veterans Health Administration (Florence, KY)
- Summary The Clinical Medical Director directly reports the Chief of Primary Care / ACOS and will be responsible for all aspects of medical care delivered to ... series. For more information, refer to Required Documents below. Responsibilities The Clinical Medical Director must be able to perform all services required in… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs , you will act as the Regional Regulatory ... 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
- Merck (North Wales, PA)
- …in those areas + US/Global experience in clinical research, regulatory affairs , scientific and medical affairs , or pharmaceutical policy + Ability to ... **Job Description** **Role Summary** + The Director Scientific Patient Engagement Lead is...preferred **Required Skills:** Client Advocacy, Clinical Research, KOL Engagement, Medical Affairs , Oncology, Patient Advocacy, Patient Insights,… more
- BeOne Medicines (San Mateo, CA)
- …North America with some activity globally. This role supports our commercial, medical affairs , legal, healthcare compliance and other business functions ... and participate on cross-functional teams for product labeling, product development teams, medical affairs , and marketing. + Provide advice on healthcare… more
- Merck (Rahway, NJ)
- …Functional Area: Regulatory Innovation and Information Management (RIIM) within Global Regulatory Affairs & Clinical Safety (GRACS) The Associate Director of ... **Job Description** **Associate Director , Regulatory Submissions Archive Operations** Location: Rahway, NJ (Hybrid role - onsite 3 days per week required)… more
- Rhythm Pharmaceuticals (Boston, MA)
- …and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible for ensuring ... commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties + Act as the… more
- GRAIL (Durham, NC)
- …development, clinical affairs , quality, or program management within the IVD, medical device, or pharmaceutical industries. + Regulatory affairs and IVD ... or biomarker development, particularly in oncology, is a plus. + Advanced scientific degree preferred. + Regulatory Affairs Certification (RAC) preferred. +… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …a **maker of possible** with us. **The Associate Director of Regulatory Affairs ** will provide regulatory support for medical device systems within infusion ... and/or R&D, including at least 5 years in Regulatory Affairs . Must have hands-on experience with complex medical...degree or higher preferred with a focus in a scientific discipline preferred + Familiarity with Infusion Pump Systems… more