TMF Coordinator

TMF Coordinator to support Oncology clinical studies at TScan Therapeutics. Responsibilities include day-to-day TMF activities in the eTMF system (uploading, classifying, quality control), serving as TMF point of contact, maintaining TMF trackers and study documentation, generating TMF metrics, ensuring compliance with ICH-GCP and FDA regulations, liaising with TMF service providers and cross-functional teams (Clinical Operations, Data Management, Medical, Safety, Regulatory, Clinical Quality), supporting audits/inspections, and exploring process improvements. Requires 2-3 years of clinical research experience, TMF filing/eTMF familiarity, knowledge of ICH-GCP and regulatory standards, strong organizational and communication skills, and ability to work in a fast-paced startup environment.