- CSL Behring (Waltham, MA)
- …a hybrid position and is onsite three days a week. You will report to the Director of Clinical Assay. You will be part of a specialized non-laboratory based team and ... key data sets to meet the business needs. Deep understanding of assay design , regulatory standards and industry best practices are essential. The incumbent will have… more
- CSL Behring (Waltham, MA)
- …position and is onsite three days a week. You will report to the Director of Clinical Assay. **Position Description Summary:** You will be part of a specialized ... key data sets to meet the business needs. Deep understanding of assay design , regulatory standards and industry best practices are essential. The incumbent will have… more
- Bristol Myers Squibb (Cambridge, MA)
- …will possess a strong scientific background, effective communication skills, and experience working in a matrixed industrial environment. Seeking candidates with ... and milestones, and manages information flow across team members **Qualifications & Experience :** + Ph.D. in Oncology/immunology or related field with + 5-8+ years… more
- Bristol Myers Squibb (Cambridge, MA)
- …+ Supports regulatory submissions and regulatory interactions as needed **Qualifications & Experience :** + PhD or MD/PhD in neuroscience with 7+ years of ... translational medicine experience + 5+ years of late-stage clinical biomarker ...required to conduct their work. This structure includes site-essential, site-by- design , field-based and remote-by- design jobs. The occupancy… more
- Bristol Myers Squibb (Devens, MA)
- …Regulatory, etc.) + GPS and Cell Therapy Franchise counterparts **Qualifications & Experience ** + BS or BA in science and/or engineering (biotechnology, biology, ... engineering, or related sciences). Prior cell therapy development operations experience is strongly preferred. + 5-8 years business experience , with 5+ years in… more
- Takeda Pharmaceuticals (Boston, MA)
- …effective medications to the patients with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality ... and ICH regulations and industry standards applicable to the design , analysis of clinical trials and regulatory submissions. +...of expertise **Education:** + PHD with ~ 5 years experience + MS with ~ 8+ years experience… more
- Takeda Pharmaceuticals (Boston, MA)
- …effective medications to the patients with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality ... and ICH regulations and industry standards applicable to the design , analysis of clinical trials and regulatory submissions. +...of expertise **Education:** + PHD with ~ 5 years experience + MS with ~ 8+ years experience… more
- Takeda Pharmaceuticals (Boston, MA)
- …us and redefine what's possible in cancer research! _ACCOUNTABILITIES_ + Design and implement automated, digitally enabled experimental workflows using robotics and ... integrated analysis platforms. + Ensure rigorous experimental design and data integrity to drive high-quality, reproducible results for drug discovery. + Collaborate… more
- Takeda Pharmaceuticals (Boston, MA)
- …diverse team whose skills, experiences, and backgrounds complement one another. Extensive experience working in Pharma or Biotech is optional. A strong curiosity for ... machine learning projects, and take a hands-on approach to steer solution design and implementation + Identify, monitor, and validate relevant external AI/ML… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …needs of Otsuka's growing portfolio. + Collaborate on MLOPS life cycle experience with MLOPS workflows traceability and versioning of datasets. Build and maintain ... including AWS, Kubernetes, Snowflake, and Dataiku **Omnichannel Optimization** + Design and deploy recommendation systems to tailor communications based on… more