Investigator Contract Lead (FSP)

Parexel; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a dedicated professional to support the ICLL site contracting workflow. You will handle CSA/CRC/ICD review and execution, align budgets with FMV principles, and coordinate with CTM, Legal, and study teams to ensure compliance.

The role demands a legal background, MS degree preferred, and 3+ years of clinical trial site contracting experience, with strong written and verbal communication, and proficient PPT skills.

Qualifications

• Legal background required.
• MS degree preferred.
• 3+ years of clinical trial site contracting experience.
• Excellent communication, writing and PPT skills.

Responsibilities

• Standard site contracting process (CSA/CRC/ICD review and execution).
• Site budgets developed aligned with FMV principles.
• Basic legal/cost negotiation with sites.
• Alignment with client SOP/legal templates.
• Coordination with CTM, Legal and study team.

Skills

Excellent Communication

Writing

PPT

Education

MS Degree preferred

Legal Background

Job description

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