Clinical Project Manager, Senior Clinical Project Manager

Summary

Join Recursion's Clinical Operations team as a Clinical Project Manager and lead the execution of clinical studies across diverse therapeutic areas. You will plan and oversee global clinical projects, manage study budgets and financial reporting, and build strong relationships with cross-functional teams and stakeholders. Ensure compliance with regulations and SOPs while managing clinical trial operations and leading study teams. This role requires a Bachelor's degree, 6+ years of clinical operations experience (including 2+ years in study management), and early-phase oncology/rare disease experience. The position is ideally based in Salt Lake City or New York City, but remote work with regular on-site visits is also considered. Recursion offers a competitive salary, bonuses, equity compensation, and a comprehensive benefits package.

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 in a study management role required
• Early phase (Phase 1, 2) oncology and/or rare disease experience at a Sponsor is required
• Demonstrated experience organizing and leading clinical study teams
• Excellent working knowledge of FDA, ICH, GCP regulations and guidelines
• Willingness and ability to travel to sites, conferences and Recursion Headquarters as needed

Responsibilities

• Lead the execution of clinical studies across diverse therapeutic areas to deliver transformative new medicines to patients
• Plan and oversee implementation, coordination, and execution of global clinical projects; including, but not limited to, oversight of study project budgets, financial reporting, and forecasting in collaboration with Clinical Outsourcing
• Develop and maintain strong relationships with cross-functional study teams, CROs, clinical investigators, and clinical trial stakeholders
• Manage clinical trial operations and lead study teams, including CROs and vendors, and reporting of start-up, conduct and close-out activities
• Ensure compliance with study protocol and applicable Standard Operating Procedures (SOP), Good Clinical Practices (GCP), ICH and local regulations

Preferred Qualifications

• Proficiency working in SmartSheet or similar project management software
• Demonstrated experience planning, initiating, conducting, and closing out phase 1 - 3 studies
• Experience in vendor and CRO selection,management, and oversight
• Experience managing and tracking study budgets and financials with participation and involvement with invoice and contract review and approvals
• Experience working closely with data management and clinical teams to set up study systems and ensure quality data collection through monitoring, cleaning and analysis (phase 1-3)
• CRF development and IRT build experience, knowledge of data listings used for monitoring and cleaning, contribution to data management related plans and specifications

Benefits

• Bonuses
• Equity compensation
• Comprehensive benefits package