Clinical Trials Administrator - FSP
Fortrea · Durham, NC
Clinical OperationsFull timeCompany career page
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Role summary
Fortrea seeks a Clinical Trial Administrator to support clinical research project execution in Durham, North Carolina. The role involves managing study documentation, coordinating with project teams, maintaining regulatory compliance, and handling administrative functions essential to trial operations.
What they're looking for
- Bachelor's degree in life sciences or related field; or Associate's degree with 2+ years relevant experience
- Minimum 1 year administrative experience in clinical research environment
- Knowledge of GCP and ICH guidelines applicable to clinical research
- Proficiency with Microsoft Office Suite and spreadsheet software
- Strong written and oral communication skills in English and local language
- Ability to work in fast-paced, matrix environment with changing priorities
- U.S. work authorization without sponsorship required
What you'll be doing
- Document and track study activities using project management systems and relevant tools
- Maintain Trial Master File documentation, participate in QC, and archive records
- Prepare, assemble, and ship study materials and supplies to investigator sites
- Coordinate investigator meetings and maintain clinical trial documentation and files
- Liaise with vendors and internal teams on study conduct, data reconciliation, and communications
Compensation$45,000-$50,000 USD
Privacy & handoff
This role links to Fortrea's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.