Senior Clinical Trial Associate

Role: Senior Clinical Trial Associate, Clinical Operations, supporting planning, execution, and management of clinical trials in a biopharma setting. Responsibilities include document tracking, maintaining inspection-ready TMF per ICH-GCP standards, assisting in study document preparation, overseeing trial supplies and shipments, and coordinating vendor invoices, contracts, and POs. The role involves supporting departmental process improvements, facilitating communication with trial sites and vendors, and participating in meetings and ad-hoc activities. Requirements: Bachelor’s in life sciences or healthcare, 4+ years of clinical research experience, strong computer skills (Excel, Word, PowerPoint, Outlook), excellent organizational and communication skills, ability to work independently, and some travel (~10%). Preferred qualifications may include experience with clinical trial coordination and vendor management. High-value specifics include work supporting Duchenne muscular dystrophy trials within a remote/hybrid setup in the US, with involvement in clinical trial logistics, documentation, and stakeholder liaison, contributing to early-phase or later-stage trials aligned with ICH-GCP guidelines.