Senior Clinical Trial Manager

Description

Your work will change lives. Including your own. Please note: Our offices will be closed for our annual Summer Break from Monday, June 29, 2026, through Friday, July 3, 2026. Our response to your application will be delayed. The Impact You’ll Make Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking a highly motivated, skilled, and adaptable Clinical Trial Manager within our Clinical Operations team who will manage the conduct and execution of one or more clinical trials from study start-up to study closure in close collaboration with the Clinical Project Manager and/or Associate Director/Director of Clinical Operations. In this role, you will: - Support the Clinical Project Manager in the execution of trial operations across diverse therapeutic areas to deliver transformative, new medicines to patients - Manage and track clinical trial activities, timelines, and deliverables - Engage and build relationships with clinical CRO and trial partners to support the successful execution of clinical trial activities - Proactively identify opportunities for operational and process improvements within the Clinical Operations team - Contribute to the advancement of the Recursion development portfolio The Team You’ll Join Reporting to an Associate Director/Director of Clinical Operations, you will be an essential member of the Clinical Operations team within Development and work closely with cross-functional study teams. You will impact all phases of Development clinical trials. The team is dedicated to ensuring operational excellence across our clinical programs. The Experience You’ll Need - Bachelor’s degree or equivalent experience - 6+ years of experience in a clinical operations role in the biopharmaceutical industry, with at least 2+ years experience as a regional CTM or similar operations role required - Preferred experience: monitoring experience, automating trial activity tracking through Smartsheet or other CTMS/tracking tools - Early phase (Phase 1, 2) oncology and/or rare disease experience at a Sponsor or CRO is required - Strong working knowledge of FDA, ICH, GCP regulations and guidelines - Effective collaboration in a fast-paced team environment - Excellent interpersonal and communication skills, and an understanding of principles of relationship management across diverse internal and external stakeholders - Detail-oriented with effective organizational and problem-solving abilities. - Experience in managing multiple priorities and able to accomplish tasks within a timeframe, setting milestones to meet deadlines and to achieve goals - Proficient in using various software applications related to clinical trials, such as, but not limited to: smartsheet, clinical trial management systems, project management tools, document management systems, and electronic