At a glanceSummarised by Seekless from the posting.
Must have3
Legal Background
At least >3 years Clinical Trial Site Contracting Experience
Excellent Communication skill, Writing and PPT
Nice to have1
Prefer MS Degree
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.
Responsibilities
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