About this role

Serve as the primary contracts professional working closely with the Clinical function
Manage the full contract lifecycle from initial draft through execution, amendment, and close-out
Draft, review, negotiate, and execute Clinical Trial Agreements (CTAs)
Coordinate Informed Consent Form (ICF) review as needed
Negotiate and process Work Orders (WOs) and Change Orders (COs)
Maintain accurate, complete, and timely contract records in Nuvalent’s contract management system

Minimum of 7 years of contracts experience in the biopharmaceutical or clinical research industry
At least 4 years focused on vendor agreements, clinical site agreements, investigator agreements, or study start-up contracting
Demonstrated experience negotiating CTAs, WOs, COs, CDAs, and HCP consulting agreements at volume
Direct experience contracting with international clinical sites
Knowledge of GCP, ICH guidelines, and FDA regulations governing clinical research
Proficiency with contract lifecycle management systems; Agiloft experience a plus
Bachelor’s degree or equivalent experience required

Senior Manager, Contracts - Clinical

Key skills