Senior Clinical Trial Manager

The Impact You’ll Make 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 data capture tools Willingness to travel to sites, conferences, and/or Recursion offices (NYC and SLC) as needed Working Location & Compensation This position is open to both remote and hybrid models. The hybrid position would be office‑based at our New York City, New York office. Employees are expected to work in the office at least 50% of the time. Relocation support can be provided for candidates not local to either geographical location. Based on the skills, experience, and qualifications needed for this role, the estimated annual base salary range is $149,820–$200,970 . In addition to base salary, this role is eligible for an annual bonus, equity compensation, and a comprehensive benefits package. Recursion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected under applicable federal, state, local, or provincial human rights legislation. Accommodations are available on request for candidates taking part in all aspects of the selection process. #J-18808-Ljbffr