Clinical Study Administrator – CTA
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Job Description
Clinical Study Administrator coordinating and administering clinical studies for Parexel. Managing documentation and stakeholder communication effectively throughout the trial process.
Responsibilities:
- Coordinate and administer clinical studies from start-up to execution and closeout
- Manage trial and site administration tasks effectively
- Interface with investigators and external service providers
- Ensure compliance with regulatory documents and application processes
Requirements:
- Clinical trial administration experience
- Knowledge of ICH-GCP guidelines
- Proficiency in document management systems
- Experience with stakeholder communication
- Ability to handle multiple tasks in a fast-paced environment
Benefits:
- Health insurance
- 401(k) matching
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