Global Site Contracts Manager - Remote

Proclinical

Boston (MA)

Remote

USD 90,000 - 150,000

Full time

2 days ago
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Job summary

Proclinical is seeking a Manager, Site Contracts in Boston (remote). You will lead end-to-end investigator site contract and budget negotiations, directly negotiating with sites and overseeing CRO partner performance to keep studies on schedule.

You’ll collaborate with Legal, Clinical Operations and Study Management to ensure contracts meet milestones and compliance. Ideal candidates have a Bachelor's degree (JD a plus) and proven experience in global site contracting, FMV budgeting, and

Qualifications

  • Bachelor's degree required; JD is a plus.
  • Experience in clinical site contracting across multiple therapeutic areas.
  • Proven ability to oversee CRO partners and ensure vendor compliance with quality standards.
  • Expertise in negotiating clinical site budgets and study-specific parameters.
  • Strong track record of managing contracting timelines for global studies.
  • Excellent collaboration with Legal, Clinical Operations, and Compliance.

Responsibilities

  • Lead site contract and budget negotiations with investigator sites and CRO partners.
  • Act as the primary escalation point for legal and financial contracting issues.
  • Ensure CRO vendors meet compliance, quality, and timeline standards.
  • Collaborate with Legal to address alternative contract language and fallback provisions.
  • Monitor contracting timelines and progress across multiple studies.
  • Build relationships with internal teams and external partners; provide SME for complex studies.

Skills

Negotiation
Cross-functional collaboration
Contract management
Budgeting
Project management
ICH-GCP familiarity
MS Office

Education

Bachelor's degree
Juris Doctor (JD)

Tools

Contract management systems
Microsoft Office Suite
Excel

Job description

Proclinical is seeking a Manager, Site Contracts in Boston (remote). You will lead end-to-end investigator site contract and budget negotiations, directly negotiating with sites and overseeing CRO partner performance to keep studies on schedule.

You’ll collaborate with Legal, Clinical Operations and Study Management to ensure contracts meet milestones and compliance. Ideal candidates have a Bachelor's degree (JD a plus) and proven experience in global site contracting, FMV budgeting, and

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