Lead the drafting, review, negotiation, and execution of contracts across clinical, development, manufacturing, commercial, and corporate activities, including clinical trial agreements, CRO agreements, investigator and site agreements, vendor contracts, partnership arrangements, strategic collaboration and license agreements, master service agreements, statements of work, commercial manufacturing agreements, and agreements with payors and pharmacies. Provide practical legal guidance to Clinical Operations and related teams in support of clinical trial start-up and execution, including matters involving clinical sites, investigators, informed consent, data privacy, study vendors, and clinical study agreements.