Clinical Trial Manager (CTM)

Clinical Trial Manager (CTM) You’ll take full ownership of your assigned trial(s) — from protocol development to close-out — with the autonomy to make daily calls and the support of an experienced team when it counts. Position Description This individual is responsible for the management of assigned clinical trial(s), leading the study team, vendors, clinical monitors, and clinical sites throughout the trial lifecycle. The Opportunity Own all operational aspects of your assigned clinical trial(s) Manage day-to-day CRO/vendor relationships to keep deliverables on budget, timeline, and protocol Build strong working relationships with site investigators and study coordinators Track trial progress and keep stakeholders updated on status Monitor enrollment and address recruitment challenges as they arise Manage study budget, forecasting, accruals, and vendor payments for your trial(s) Partner with Data Management on CRF content, completion guidelines, and data deliverables Draft and coordinate review of protocols, informed consents, CRFs, monitoring plans, and study reports Prepare for and support regulatory agency audits and inspections Flag risks early and recommend solutions before they become problems Represent Clinical Operations at project team meetings What You’ll Bring S./B.A. in biological sciences with 5+ years of relevant industry experience Ability to travel as required for the program (25%) Working knowledge of FDA, EMA, ICH, and GCP regulations and guidelines Experience managing trials independently from start-up through close-out Comfortable leading day-to-day CRO/vendor relationships Strong analytical and problem-solving skills Clear, confident communicator who can create direction for a study team Ability to manage time demands, incomplete information, and shifting priorities Highly organized, able to multi-task and prioritize independently Thrives in a fast-paced, small-company environment Salary Range: $157,700 - $168,200 annually The posted range appl