Clinical Trial Associate
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Job Summary
Joining a dynamic team, the full-time remote Clinical Trial Associate will assist in eTMF filing, support study teams with TMF functionality, and coordinate logistics for meetings and training.
Key responsibilities
- Assist in eTMF filing and administration, ensuring document completeness and conducting final site-level reviews
- Support study teams with TMF functionality in accordance with study-specific plans and processes
- Coordinate logistics for meetings, events, and training, and participate in project team meetings while maintaining action logs
Required qualifications
- Bachelor's degree or international equivalent in a clinical, biological, scientific, or health-related field, or equivalent experience
- 0 to 2 years of practical experience in clinical trial administration, such as Inhouse CRA or site administration
- Knowledge of ICH/GCP and/or ISO14155 requirements and relevant country-specific regulatory requirements
- Strong analytical and organizational skills, with the ability to manage multiple projects in a fast-paced environment
- Excellent English verbal and written communication skills
Complete Job Description
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