- Dana-Farber Cancer Institute (Boston, MA)
- …of study records, and resolution of data queries. + Prepare and or complete regulatory related reports and IRB submissions . Maintain and organize study ... in the clinical trial setting and identifying potential targets for intervention. The Senior CRC supports the research team in the overall conduct of clinical trials… more
- Beth Israel Lahey Health (Boston, MA)
- …the progress of protocols; planning and prioritizing the work. Management of regulatory aspects of the study, including interaction with Institutional Review Board. ... regarding ambiguous or incomplete data. Monitors quality and timeliness of data submissions . Ensures data extracts completed by staff are in compliance with… more
- Novo Nordisk (Lexington, MA)
- …in vitro studies to provide insights and recommendations internally and externally, including regulatory submissions . + Ensures data integrity so that the in ... in communicating and presenting scientific data internally, externally, and in regulatory submissions + prior experience working in cross-disciplinary research… more
- Olympus Corporation of the Americas (Westborough, MA)
- …materials, processes, manuals, plans, committees, study systems and all sponsor required regulatory submissions . + Owns and manages the clinical trial budget ... strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures. + Tracks development of and… more