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Clinical Research Monitor (CRA)
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- We're looking for a Clinical Research Monitor(CRA) , working in Healthcare Systems and Services industry in Minneapolis, Minnesota, United States
- Monitors progress of clinical trials at the site level or headquarters and ensures that they are conducted, recorded and reported in accordance with the protocol, standard operating procedures (SOP), good clinical practices (GCP), and other applicable regulatory requirements.
- Includes headquarter and field clinical research associates (CRA).
- Conduct centralized monitoring activities across the various phases of the trial associated with the study planning, start-up, execution, closeout, of clinical trials utilizing OC-RDC and CTMS (and additional electronic platforms as needed).
- Maintain oversight of key operational risk indicators (trial and site level); investigate and mitigate potential trial risks.
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