- Dana-Farber Cancer Institute (Brookline, MA)
- …Trials Offices at the various DF/HCC institutions. The Institutional IND Regulatory Coordinator works directly for the Clinical Trials Office to complete and ... agencies, and other research organizations. Works interactively with the Office for Human Research Studies (OHRS), ...continuing reviews, and informed consent documents for SRC and IRB review and approval. + Prepares and… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval + Prepares and submits regulatory documentation ... pharmaceutical industry, federal agencies, and other research organizations. Works interactively with the Office for Human Research Studies (OHRS), Office of… more
- Dana-Farber Cancer Institute (Boston, MA)
- …scientists, patients, and administrative stakeholders, including OnCore Data Informatics team and Office for Human Research Studies (OHRS). The CRC II will ... the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. +… more
- Beth Israel Lahey Health (Boston, MA)
- **Overview** The purpose of the **Clinical Research Coordinator I** is to coordinate clinical research activities for the Joslin 50-year Medalist Study, which was ... + Assists in making amendments to protocols and submit proper documentation to IRB . + Performs other duties as needed. **Qualifications** + Bachelor's Degree + 0-3… more
- Veterans Affairs, Veterans Health Administration (Boston, MA)
- …scientific research teams to successfully onboard research projects, including completion of Institutional Review Board ( IRB ) applications. Collaborates ... the Million Veteran Program (MVP) within the Veterans Affairs Office of Research and Development. The position is located...The Health Science Specialist serves as a research project coordinator and has full charge of maintaining a comprehensive,… more