- Bristol Myers Squibb (Princeton, NJ)
- …+ Work as part of cross-functional teams-including clinical development, medical affairs , regulatory , and biostatistics-to ensure HEOR contributions are ... patient/clinician reported measures across Cell Therapy portfolio. Support the Executive Director in developing and executing health economic & outcomes research… more
- Otsuka America Pharmaceutical Inc. (Salem, OR)
- …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... **Associate Director , Small Molecule Analytical Development** + Lead and...and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols… more
- Lilly (Indianapolis, IN)
- …+ **Collaborate Across Functions:** You will partner closely with Quality Operations, Regulatory Affairs , IT, and Global Inspection Readiness to align on ... Global Data Analytics & AI Organization (DIA) is actively seeking an **Associate** ** Director of Data, Analytics & AI (Quality)** to lead the digital transformation… more
- AbbVie (North Chicago, IL)
- …Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Associate Director , Statistics provides statitical leadership for clinical development and ... of work may include clinical trials, patient safety, and global medical affairs . The Associate Diector works in partnership with experts in multiple disciplines… more
- Fujifilm (College Station, TX)
- …Collaboration** : Work closely with the Quality Assurance, Manufacturing, and Regulatory Affairs teams to support product development and ensure ... **Position Overview** As the Associate Director of Microbiology, you will play a pivotal...a contamination-free environment, support our product pipeline, and ensure regulatory compliance. **Company Overview** The work we do at… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the quality ... and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports Takeda's… more
- AbbVie (Irvine, CA)
- …to providing the most comprehensive science-based product offerings available. The Director II, Clinical Development will oversee the direction, planning, execution, ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues.… more
- BeOne Medicines (Emeryville, CA)
- …development. This role partners closely with Clinical Pharmacology, Clinical Biomarker, Regulatory Affairs , and Clinical Development to ensure robust study ... **General Description:** The Director of Biostatistics will provide strategic statistical leadership for pharmacokinetic (PK) and pharmacodynamic (PD) studies across… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory ... company that will inspire you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. Our Data and… more
- AbbVie (South San Francisco, CA)
- …team physicians, epidemiologists, safety analysts), Statistical Programming, Clinical Statistics, Regulatory Affairs , and Medical Writing. Safety Statisticians ... Oncology TA Head in our Safety Statistics team. The Director will have oversight of statisticians in oncology. This...+ Provide strategic input on safety related submissions to regulatory agencies and responses to requests from regulatory… more