Clinical Trial Associate
Job Summary
Supporting biotech, medtech, and specialty pharma companies, the full-time remote Clinical Trial Associate I will assist with eTMF filing, coordinate study team logistics, and participate in project meetings to ensure compliance and efficiency in clinical trials.
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 while maintaining action and decision logs
Required qualifications
- Bachelor's degree or international equivalent in a clinical, biological, scientific, or health-related field
- 0 to 2 years of experience in clinical trial administration preferred
- Knowledge of ICH/GCP and/or ISO14155 requirements, along with 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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