Site Contract Management
上海, 中国
职位描述
Job Overview
Manage the end-to-end process of clinical trial agreements and budgets (preparation, negotiation, finalization), while providing site/investigator budget and contract support to clinical teams.
Key Responsibilities
Prepare, negotiate, and finalize clinical trial agreements and ancillary contracts for sponsored/investigator-initiated studies via direct site negotiations or CRO oversight.
Analyze contractual terms and budget risks in collaboration with global teams, legal, and compliance stakeholders; escalate issues appropriately.
Ensure investigator compensation aligns with fair market value and regional standards.
Support negotiations for confidentiality agreements, informed consent forms, and ancillary documents.
Manage contract amendment lifecycle and track key metrics.
Optimize processes to reduce site activation cycle times and improve efficiency.
Oversee site payment reviews to ensure compliance with study costs and guidelines.
Maintain audit-ready documentation per regulatory requirements and internal policies.
Ensure timely execution of deliverables within established targets.
Qualifications
Bachelor's Degree, 0-2 years' working experience
Ability to assess legal/financial risks and collaborate cross-functionally.
Process improvement mindset with strong analytical skills.
Professional English proficiency required.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
