- 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
- Beth Israel Lahey Health (Boston, MA)
- …sponsored research post-award portfolio including oversight and management of financial policy, compliance and reporting issues that arise during the life of the ... to ensure they operate within financial limitations as well as their compliance with legal, sponsor and Center policies and procedures. Position also supports… 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