SR. Trial Master File Specialist

Maintain the electronic Trial Master File (eTMF) in accordance with ICH-GCP and SOPs Perform TMF quality checks for completeness, accuracy, currency, and consistency Track missing/incomplete documents and follow up with internal teams, CROs, and sites Support study startup, maintenance, and close-out activities from a TMF perspective Bachelor’s degree in life sciences or related field 2–5+ years in clinical trials, TMF management, or clinical operations Strong working knowledge of ICH-GCP and global regulatory requirements Experience with eTMF systems (e.g., Veeva Vault eTMF, Wingspan, MasterControl) Excellent attention to detail and document quality 100% employer-paid medical, dental, and vision premiums for you 401(k) with employer match Pre-tax commuter benefits (transit/parking) Flexible Spending Accounts (FSA) Hybrid work model with flexibility Flexible, take-what-you-need PTO and company holidays