- Sartorius (Marlborough, MA)
- …antibody engineering and manufacturing processes that can be transformed from early pre- clinical stage into cGMP ready manufacturing scale. The incumbent is expected ... This exciting initiative enables the research, process development and clinical production of novel modalities using next generation manufacturing platforms,… more
- Bristol Myers Squibb (Cambridge, MA)
- …physicians + May serve as CTP as necessary + Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each study led by ... enterprise disease area portfolio + CDL has demonstrated, sustained excellent performance as Clinical Trial Physician, Clinical Scientist , or equivalent +… more
- Bristol Myers Squibb (Cambridge, MA)
- …eligibility review + Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including ... strategic oversight in protocol development (input on inclusion/exclusion and other safety -related clinical considerations) + Fulfills GCP and compliance… more
- Bristol Myers Squibb (Cambridge, MA)
- … clinical lifecycle + Manages site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety ... strategic oversight in protocol development (input on inclusion/exclusion and other safety -related clinical considerations) + Fulfills GCP and compliance… more
- Takeda Pharmaceuticals (Boston, MA)
- …cases may lead the US/EU Development Team but more likely will oversee the clinical scientist (s) responsible for leading this team. Emphasis will be on insuring ... shine? Join us as a Senior Medical Director, Oncology Clinical Science in our Cambridge office. At Takeda, we...assessing issues related to protocol conduct and/or individual subject safety . Assesses overall safety information for studies… more
- Sanofi Group (Cambridge, MA)
- … trial conduct (DRSR, safety , stat outputs of blinded data, ) with clinical scientist , bio stat and GSO + Lead the study specific committees (IDMC, ... **Job Title:** Clinical Lead, I&I **Location** : Cambridge, MA or...questions raised by EC/IRBs, sites **Contribution to regulatory and safety documents and meetings:** + Represents his/her project at… more
- Merck (Boston, MA)
- …and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study ... **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and...) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in… more
- Merck (Boston, MA)
- …and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study ... **Job Description** The Executive Director (Distinguished Scientist ) has primary responsibility for the planning and...has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in… more
- Takeda Pharmaceuticals (Boston, MA)
- …the US/EU Development Team but more likely will oversee the study physician and/or clinical scientist leads responsible for leading the team. Emphasis will be on ... empower you to shine? Join us as a Executive Medical Director, Oncology Clinical Sciences in our Cambridge office. At Takeda, we are transforming the pharmaceutical… more
- Charles River Laboratories (Shrewsbury, MA)
- …regulatory guidelines that apply to the recording of study data. Interact with Scientist , QA staff and other departments with regards to data. **ESSENTIAL DUTIES AND ... that they are completed correctly. * Communicate with department management and Scientist regarding any issues related to data collection that impact the recording… more