Recursion - Senior Clinical Trial Manager
Requirements
• 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
Responsibilities
• Support the Clinical Project Manager in the execution of trial operations across diverse therapeutic areas to deliver transformative, new medicines to patients • Support • Manage and track clinical trial activities, timelines, and deliverables • Manage and track • Engage and build relationships with clinical CRO and trial partners to support the successful execution of clinical trial activities • Engage and build • Proactively identify opportunities for operational and process improvements within the Clinical Operations team • Proactively • Contribute to the advancement of the Recursion development portfolio • Contribute • 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.
Benefits
• This position is open to both remote and hybrid models. The hybrid position would be office-based at our London, England office near King's Cross. 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. • remote and hybrid
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