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Job Description
Structured overview of role & requirementsAbout This Role
Lead negotiation, execution, and management of Clinical Trial Agreements (CTAs) and site budgets with investigative sites.
Collaborate with Clinical Operations and Project Management teams to support timely site activation and track contract execution timelines.
Ensure compliance with local laws and regulatory requirements while mitigating legal and operational risks throughout clinical trial start-up and contract lifecycle.
Minimum Requirements
Bachelor’s degree in Life Sciences or related discipline, or equivalent experience.
3+ years experience in negotiating and managing clinical trial contracts and site budgets within pharmaceutical, biotech, or CRO environments.
Strong understanding of regulatory and compliance requirements for clinical trials across jurisdictions.
Work Experience Required: 3+ years in relevant domain.
Ideal Candidate Profile
Experienced in managing multiple contracts and priorities in fast-paced clinical trial environments with ability to meet deadlines.
Capable of applying regulatory compliance knowledge to minimize risks and ensure contract adherence globally.
Has skill in mentoring junior staff and collaborating effectively within cross-functional teams focused on site activation and clinical operations.