Clinical Trial Associate I

Job Summary

Supporting the Functional Services Provider (FSP) team, the full-time remote Clinical Trial Associate I (TMF) will assist in eTMF filing and administration, coordinate study team logistics, and participate in project meetings to facilitate clinical trial processes.

Key responsibilities

• Assist in eTMF filing and administration, ensuring document completeness and conducting final site-level reviews
• Support the study team with the functionality and use of TMF in accordance with study-specific plans and processes
• Coordinate logistics for meetings and training, and prepare meeting minutes while maintaining action/decision 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 (e.g., Inhouse CRA, CTA, site administration)
• Knowledge of ICH/GCP and/or ISO14155 requirements, as well as country-specific regulatory requirements for clinical trials
• Strong analytical and organizational skills, with the ability to manage multiple projects in a fast-paced environment
• Proven ability to deliver quality and timely results through positive customer interactions