Clinical Trial Associate
Job Summary
To support the execution and delivery of clinical trials, the full-time Clinical Trial Associate will manage study start-up activities, maintain trial documentation, and ensure compliance with regulatory requirements while working in a hybrid environment.
Key responsibilities:
- Manage the execution of the CDA process and coordinate site feasibility questionnaires
- Collect and organize essential documents for site activation and maintain trial documentation in compliance with SOPs
- Ensure the collection of site trial eTMF documentation during study close-out and assist in final reconciliations
Required qualifications:
- Bachelor's degree in health, biological science, or a related field
- 1 year of related experience in clinical research or a comparable combination of education and training
- Familiarity with Good Clinical Practices (GCP), ICH guidelines, and FDA regulations
- Technical skill in clinical software, such as CTMS, is preferred
- Basic knowledge of CRO clinical systems and procedures
Complete Job Description
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