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Global Site Contract Lead​/Senior Site Contract Lead

Job in New York, New York County, New York, 10261, USA
Listing for: Parexel
Contract position
Listed on 2026-10-15
Job specializations:
  • Business
    Regulatory Compliance Specialist, Operations Management
Salary/Wage Range or Industry Benchmark: 140000 - 190000 USD Yearly USD 140000.00 190000.00 YEAR
Job Description & How to Apply Below
Position: Global Site Contract Lead / Senior Site Contract Lead
Location: New York

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.

About the Role

Parexel is seeking an experienced Global Site Contract Lead (SCL)/Senior Site Contract Lead (SSCL) to drive excellence in clinical trial site contracting. These levels require people with experience leading site contracting across multiple countries and regions in a sponsor-facing capacity.

The role is based remotely in the following countries which you must be living and have the right to work in:
Croatia Czech Republic Georgia Hungary Lithuania Poland Romania Serbia Ukraine

What You'll Do
  • Lead end-to-end site contracting for clinical trials, ensuring timely and effective contract execution
  • Monitor and report on critical metrics including cycle times, contract quality, and compliance throughout the contract lifecycle
  • Develop and implement contracting strategy documents, templates, and best practices that drive efficiency and consistency
  • Collaborate with global teams on investigator grant budgets and fee parameters
  • Manage project-specific contracting teams, providing leadership, training, and mentorship
  • Identify and mitigate risks related to timelines, budgets, strategy effectiveness, and quality
  • Maintain transparent communication with all stakeholders—sponsors, internal teams, vendors, CROs, and sites
  • Build and strengthen relationships across internal and external partners to expedite contract execution
  • Support cross-functional teams including Clinical Operations, Feasibility, Business Development, and Investigator Payments
  • Provide regular performance updates and insights to clients and senior management
  • Ensure accurate budget tracking and resource forecasting for the contracting team
What We're Looking For
  • Very strong global site contracting experience within a CRO or other clinical research setting
  • Experience leading site contracting across multiple countries and regions
  • Bachelor's degree in law, business, economics, or related field (or equivalent industry experience)
    Strong negotiation and contract management skills with ability to interpret complex legal language
  • Excellent leadership, diplomacy, and interpersonal skills with proven ability to influence across teams

    Outstanding organizational and project management abilities—comfortable juggling multiple concurrent projects
  • Advanced proficiency in Excel, Word, and Power Point Strong  analytical skills and attention to detail
  • Experience with contract management systems and eTMF platforms

    Ability to thrive in virtual, multicultural, and cross-timezone environments
  • Demonstrated thought leadership, problem-solving ability, and grace under pressure
Why Join Us?

You’ll take ownership of a critical function that directly impacts trial success, working with talented cross-functional teams and gaining exposure to diverse therapeutic areas and global operations.

Position Requirements
10+ Years work experience
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