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Jobs at Parexel

Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

Site Contract Lead / Senior Site Contract Lead

Job ID R0000045176 , Serbia

About the Role

Parexel is seeking an experienced Site Contract Lead (SCL)/Senior Site Contract Lead (SSCL) to drive excellence in clinical trial site contracting. You'll oversee the complete contracting lifecycle—from strategy and negotiation through execution and performance monitoring—while streamlining processes, controlling costs, and managing risks. As a key orchestrator, you'll ensure internal teams, sponsors, sites, and external partners stay aligned and focused on delivering successful clinical trials.

The role is based remotely in the following countries which you must be living and have the right to work in:

Serbia

Poland

Ukraine

Romania

Hungary

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

  • 3 to 8 years of experience (depending on level)​within a CRO or related field

  • 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 PowerPoint

  • 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.


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