Job Summary
A clinical staffing agency has a current position open for a Remote Trial Master File Operations Associate I.
Must be able to:
- Escalate any TMF Quality issues in a timely manner
- Perform all QC related tasks
- Ensure document quality and compliance through active engagement with clinical study teams
Skills and Requirements Include:
- 2 years of progressively relevant experience in a pharmaceutical, biotechnology or related environment
- Bachelors degree or equivalent
- Working knowledge of the Drug Information Association
- Working knowledge of ICH E6 Section 8 Essential Documents and Good Documentation practices