
Senior Manager, Contracts - Clinical
Posted May 7

Posted May 7
This is a fully remote position, open to applicants in Massachusetts.
• Act as the lead contracts expert collaborating closely with the Clinical department.
• Oversee the entire contract lifecycle from the initial draft to execution, amendments, and final closure.
• Draft, assess, negotiate, and finalize Clinical Trial Agreements (CTAs).
• Organize the review of Informed Consent Forms (ICFs) as necessary.
• Negotiate and manage Work Orders (WOs) and Change Orders (COs).
• Ensure accurate, complete, and timely documentation of contracts in Nuvalent’s contract management system.
• A minimum of 7 years of contracts experience within the biopharmaceutical or clinical research sector.
• At least 4 years dedicated to vendor agreements, clinical site agreements, investigator agreements, or study start-up contracts.
• Proven expertise in negotiating CTAs, WOs, COs, CDAs, and HCP consulting agreements at a high volume.
• Direct experience in contracting with international clinical sites.
• Familiarity with GCP, ICH guidelines, and FDA regulations related to clinical research.
• Competency in using contract lifecycle management systems; experience with Agiloft is a plus.
• Bachelor’s degree or equivalent experience is required.
• Medical, dental, and vision insurance.
• 401(k) retirement savings plan.
• Generous paid time off.
• Company-wide shutdown during summer and winter.
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