- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with 8-10 years pharmaceutical industry experience with 4+ years direct or related CMC regulatory experience or + PhD. with 6-8 years pharmaceutical industry ... Leads US FDA/EU EMA interactions with support from higher-level manager . + ** Regulatory Knowledge:** Demonstrates expert knowledge...experience and 4+ years direct or related CMC regulatory experience + Successful track record… more
- Frontier Medicines (South San Francisco, CA)
- Join Frontier Medicines on an exciting journey as our newest Senior Manager / Associate Director in CMC Development, located at either our Boston or South San ... of our team, reporting directly to the Head of CMC , you'll play an integral role in advancing our...thorough understanding of ICH guidelines, GLP/GMP manufacturing, and related regulatory requirements is required + Ability to travel domestically… more
- Schrodinger (Cambridge, MA)
- We are looking to hire a **Senior Manager / Associate Director of Clinical Pharmacology** to join us in our mission to discover and develop drugs that improve ... stakeholders including DMPK, translational medicine, clinical development, clinical operations, regulatory , CMC , and project management to ensure completion… more
- BeiGene (San Mateo, CA)
- **General Description:** The Associate Manager of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and ... and provide a high service level to internal stakeholders (eg Clinical Operations, Regulatory , Quality, CMC ). + Work with Clinical Operations to understand… more
- BeiGene (Hopewell, NJ)
- **General Description:** Sr. Manager / Associate Director, Supply Chain CMO Management & PM will own and enable the communication, coordinate tasks between the ... with Contract Manufacturers (CMO) + In partnership with Quality, CMC , Procurement, ensures that innovation, manufacturing performance, cost objectives and… more
- Merck (North Wales, PA)
- …the Research & Division organization of our company. **Position Description/Summary:** The GPAM Associate Director, Project Manager , is a core member of Early ... **Job Description** The drug development Project Manager is part of Global Project and Alliance...strategic and tactical input from diverse disciplines (eg, clinical, regulatory , market access, manufacturing, CMC , commercial, and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …our team, **Biologics Pre-Pivotal Formulation and Process Development** , as an ** Associate Scientist** . The successful candidate will contribute to the development ... documentation practices. . Author technical documents such as protocols, reports, regulatory dossier, etc. and prepare data-focused presentations for internal and… more
- Takeda Pharmaceuticals (Boston, MA)
- …Previous drug development experience is preferred (eg Medical Affairs, Clinical Research, Regulatory , CMC , or other development related function) + Project ... order to enhance team effectiveness and efficiency, + The Associate Director works closely together with the Oncology Business...+ 5 to 7 years experience as a project manager leading complex pharmaceutical projects in a multi-disciplinary, global… more
- IQVIA (Durham, NC)
- …ancillary supply related questions in close collaboration with the Ancillary Support Associate (ASA)/ Site Manager (SM). + Develop IP administration training ... Investigational Product Specialist, Site Investigational Product Specialist, Ancillary Support Associate , Independent Drug Monitor Manager , Independ ent Drug… more
- Blue Cross and Blue Shield of Louisiana (Baton Rouge, LA)
- …and documenting information and working closely with the Medical Directors and Manager of Medical Policy and Medical Appeals to ensure successful fulfillment of ... does not manage people + This role reports to this job: MANAGER , MEDICAL POLICY + Necessary Contacts: Benefits Administration, Network Administration, Information… more