Discover a career
with greater purpose

• 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.