Contract Clinical Research Associate

Location
San Francisco, CA
Posted
Jan 17, 2019
Required Education
Bachelors Degree
Position Type
Contract

Job Description:

CTT is seeking a contract clinical research associate (CRA) to monitor a Phase 1 clinical trial. The CRA will assist in validating the eCRF database, conduct site initiation, interim clinical monitoring and close out visits. The CRA will also assist in investigating any safety events associated with a clinical trial. Prior experience as a contract clinical research associate is essential. Home-based location.

Responsibilities for the Clinical Research Associate

  1. Participate in relevant training from eCRF database company
  2. Review eCRF content for completeness/appropriateness
  3. Assist in testing the eCRF database by the contracted organization and Study Sponsor
  4. Conduct Site Initiation Visit, Interim Clinical Monitoring Visits and Close Out Visits at trial site (traditional monitoring scheme)

Requirements for the Clinical Research Associate

  1. This is a contract position; prior experience as a contractor is required
  2. The candidate must have significant experience as a clinical research associate