Senior Manager, Clinical Contracts
$170,000–$182,000 year
HybridSan Diego, California, United States
Job Summary
Provide comprehensive contract lifecycle management by working with Clinical Operations, Legal, Finance, and stakeholders to support the timely initiation, negotiation, risk assessment, and execution of clinical trial agreements. Manage tracking of contracts, amendments, and budgets while serving as the point person for internal and external stakeholders. Establish contracting SOPs, support RFx and vendor management activities, and facilitate contract actions independently to expedite processes. Build strong relationships with investigators and vendors, respond promptly to inquiries, and ensure compliance with regulatory guidelines and QA requests. Identify process improvements to enhance efficiency and maintain clear communication across cross-functional teams.
Required Qualifications
- Bachelor's degree
- 8+ years of contract management experience within the biotechnology or pharmaceutical industry
- Clinical Site Budget experience
- Strong experience with global Phase 1-3 clinical trials
- Good knowledge of ICH-GCP, pharmaceutical related regulations and laws
- Proficiency in Microsoft Excel at an Intermediate level
- United States work authorization
- Ability to relocate to San Diego and/or report in office 5 days per week
- Willingness to travel to San Diego on a monthly basis or as needed
Desired Qualifications
- Experience within academia or a Clinical Research Organization (CRO)
- Oncology clinical trial experience
- Grant Plan experience
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