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Regional CRA
The RS-CRA will be directly responsible for conducting site qualification, initiation, interim monitoring and study closeout visits in accordance with all applicable regulations, guidelines, and business processes and will monitor the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas. Report monitoring activities and study site conduct via written reports. Interact and build professional and collaborative relationships with all study personnel, peers and office-based personnel.
Clinical Research
About Me
Industry: |
Research |
|---|---|
Occupation: |
Clinical Research |
Education level: |
Bachelor |
Will Relocate: |
Yes |
Location: |
Baton Rouge, LA |
