Job Summary
A pharmaceutical research and consulting firm has a current position open for a Remote Clinical Site Activation Partner.
Individual must be able to fulfill the following responsibilities:
- Register investigator sites in egistries as required
- Assist with study site activation activities to ensure timely site activation
- Support and/or coordinate central Investigator Review Board (IRB) submissions
Skills and Requirements Include:
- Minimum of 2 years of related experience
- Clinical trials support or pharmaceutical industry experience required
- Experience with PC-Windows, word processing, and electronic spreadsheets required
- Knowledge of ICH and local regulatory authority drug research and development regulations required
- Demonstrated knowledge of global and local regulatory requirements
