- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the ... develop the drug in accordance with a clinical and regulatory strategy. + Working with experts and consultants in...writing). + An advanced understanding of clinical medicine and science . + Advanced understanding of drug development principles and… more
- Coinbase (Boston, MA)
- …Risk/Credit Risk/Account Take Over models. * MS in Machine Learning, Computer Science , other technical field ( PhD preferred) * Strong developer experience ... work effectively with domain experts Nice to have: * Familiarity with regulatory requirements in financial services * Knowledge of crypto/blockchain technology Job… more
- Bristol Myers Squibb (Cambridge, MA)
- …computational biologists, contract research organizations and translational scientists to deliver science that supports the development of medicines to patients in ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
- Tufts Medicine (Boston, MA)
- …Core Laboratory. The Core Laboratory Director's responsibilities include technical, regulatory , and clinical oversight of various core laboratory disciplines, such ... and appropriate board certification (DABCC or NRCC), while physicians (MD or MD/ PhD ) should have board certification in Clinical Pathology. **How you'll transform… more
- Amgen (Cambridge, MA)
- …longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities ... reports, analytical method descriptions and analytical CMC sections in regulatory documents + Lead project teams and/or project sub-teams...5 years of Scientific experience; Or + Doctorate degree PhD OR PharmD OR MD and 2 years of… more
- Sanofi Group (Cambridge, MA)
- …for safety analysis, including quality, relevance to external stakeholders (eg regulatory authorities, medical journals), and scientific validity. + Accountable for ... promote state-of-the-art methodology and standards for safety analyses. **About you:** + PhD /MS in statistics or related discipline with 6 years of pharmaceutical… more
- Bristol Myers Squibb (Cambridge, MA)
- …Methodology and Innovation function within Global Biostatistics and Data Science organization. They will engage with Biostatisticians and other cross-functional ... solutions to statistical innovation problems identified by Global Biostatistics and Data Science organization. Key responsibilities of this position are focused on 3… more
- Sanofi Group (Cambridge, MA)
- …Our Medical function serves as a key strategic partner with commercial, regulatory , clinical, and market access on therapeutic solutions to support patients' needs. ... needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a...+ Advance degree in life sciences or pharmaceutical sciences ( PhD , PharmD, MD) **Experience:** + Minimum of 2 years'… more
- Sanofi Group (Waltham, MA)
- …to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions ... least 8+ years of experience in the pharmaceutical industry. PhD is preferred. + Strong experience in vaccine or...Strong knowledge of product and process development, cGMPs, and regulatory requirements across all stages of product development +… more
- Danaher Corporation (Waltham, MA)
- …you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential-one discovery at a time. Learn about the Danaher ... clients and senior management. The essential requirements of the job include: + PhD in molecular biology, biochemistry, or related discipline with 3+ years of… more