- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …: Plan, conduct, and report GCP audits of CROs, clinical laboratories, and investigator sites globally, ensuring compliance with ICH-GCP, local regulations, and ... : Maintain audit metrics and contribute to management reporting on audit outcomes, trends, and compliance risks. **Qualifications** Required + Bachelor's… more
- Parexel (Boston, MA)
- …the quality of investigator sites (eg patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and ... the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance… more
- Parexel (Boston, MA)
- …the quality of investigator sites (eg patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and ... the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance… more
- Beth Israel Lahey Health (Burlington, MA)
- …between sponsors and investigators in all aspects of study start up. 3 ) Implements assigned research studies by reviewing study and assessing protocol and ... and communicates study procedures with collaborating departments to ensure compliance with all study requirements; conducts in-services (eg arranges special… more
- Dana-Farber Cancer Institute (Boston, MA)
- …trials using Good Clinical Practice under the auspices of the Principal Investigator . These positions, in collaboration with the program's Clinical research Managers ... group's clinical trial portfolio and all related regulatory and compliance requirements. + The ACRM will assist the CRM...+ Assists the study team to be maintain an " audit ready" research environment **Data Management & Clinical Trial… more