Investigator Contract Lead (FSP)
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
ICLL is responsible for site contracting (CSA, CRC) cost effectiveness, contract integrity, and site financial governance:
- Standard site contracting process (CSA / CRC / ICD review & execution)
- Site budget development aligned with Fair Market Value (FMV) principles
- Basic legal/cost negotiation with sites
- Alignment with client SOP / legal templates
Coordination with CTM / Legal / study team
Minimal/Must-have Requirement
1. Legal Background
2. Prefer MS Degree
3. At least >3 years Clinical Trial Site Contracting Experience
4. Excellent Communication skill, Writing and PPT
This role requires you to be in China-Shanghai-Remote. If that means relocating or flying in, it is worth checking fares before you commit to a start date.
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