- Amgen (Washington, DC)
- …this. Let's change the world. Amgen is seeking a Regulatory Affairs Director supporting products in the Oncology Therapeutic Area. Global Regulatory ... It's time for a career you can be proud of. ** Regulatory Affairs Director - Global Regulatory Leader - Oncology ** **Live** **What you will do**… more
- Takeda Pharmaceuticals (Washington, DC)
- …FDA/EMA/PMDA regulations; ICH guidance; GLP/GCP requirements; SEND requirements, etc.). + Regulatory Affairs Credential (RAC-Drugs) is an advantage. + Strong ... the best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology and… more
- Takeda Pharmaceuticals (Washington, DC)
- …partner with Marketing, Patient Value & Access (PVA), Strategic Account Managers and Medical Affairs . + The National Sales Director (NSD) for the lung franchise ... Description** **About the role:** As a member of Takeda Oncology , your work will contribute to our bold, inspiring...Value & Access (PVA), Strategic Account Managers and Medical Affairs as well as across other sales franchises. **How… more
- AbbVie (Washington, DC)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director , Reimbursement, Government Affairs is responsible for monitoring ... remarkable impact on people's lives across several key therapeutic areas - immunology, oncology , neuroscience, and eye care - and products and services in our… more
- Amgen (Washington, DC)
- …the world's toughest diseases. With our focus on four therapeutic areas - Oncology , Inflammation, General Medicine, and Rare Disease- we reach millions of patients ... of patients while transforming your career. Clinical Research Medical Director **What you will do** Let's do this. Let's...you will have an opportunity to shape the Thoracic Oncology Therapeutic Area. This role will report directly to… more
- Amgen (Washington, DC)
- …quality challenges that could impact results or timelines. + Solid understanding of regulatory guidelines in oncology drug development. + Staying current in ... of life cycle (pre-clinical, clinical and post-marketing). + Prior experience with oncology drug development. + Statistical experience with regulatory and… more
- Amgen (Washington, DC)
- …Collaboration:** Partner with departments like Manufacturing, Supply Chain, IT/DTI, Regulatory Affairs , and Quality Assurance to streamline data ... understanding of pharmaceutical industry operations, including manufacturing, supply chain, regulatory compliance, and quality control. The Associate Director … more