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Parexel Site Contract Lead / Senior Site Contract Lead Recruitment 2026: Apply Online | jobscheck.in

⏳ Last Date to Apply: Open Until Filled

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Parexel

Parexel Site Contract Lead / Senior Site Contract Lead Recruitment 2026: Apply Online

Site Contract Lead / Senior Site Contract Lead

📍 Location: Serbia (Remote / Home-based across Croatia, Czech Republic, Hungary, Lithuania, Poland, Romania, Serbia, and Ukraine)
💼 Type: Full-Time
💻 Work Mode: Remote
Experience Required
3 to 8 Years
Salary / Package
Competitive & Market Standard
Work Mode
Remote
Openings
Multiple

Job Overview

  • Drive excellence in clinical trial site contracting by overseeing the entire contracting lifecycle from initial strategy and drafting to negotiation and final execution.
  • Monitor and report on critical operational metrics including turnaround cycle times, contract quality, and regulatory compliance.
  • Establish contracting strategy documents, standard templates, and industry best practices to foster operational efficiency.
  • Collaborate closely with global teams regarding investigator grant budgets, financial parameters, and resource forecasting.
  • Manage project-specific contracting teams, offering mentorship, professional training, and proactive risk mitigation.
  • Maintain clear, transparent communication channels with sponsors, investigative sites, external vendors, and internal stakeholders.
  • Support cross-functional departments such as Clinical Operations, Business Development, Feasibility, and Investigator Payments.

Key Job Details

Company NameParexel
Job RoleSite Contract Lead / Senior Site Contract Lead
Experience3 to 8 Years
Salary RangeCompetitive & Market Standard
Job TypeFull-Time
Work ModeRemote
OpeningsMultiple
Job LocationSerbia (Remote / Home-based across Croatia, Czech Republic, Hungary, Lithuania, Poland, Romania, Serbia, and Ukraine)

Key Responsibilities

  • Manage end-to-end site contracting and negotiations for international clinical trials.
  • Track and optimize key contracting metrics, cycle times, and compliance standards.
  • Develop robust contracting strategies, document templates, and operational best practices.
  • Collaborate with global internal teams and external sponsors on investigator grant budgets.
  • Provide leadership, guidance, and mentorship to project-specific contracting teams.
  • Identify and mitigate risks relating to project timelines, budget allocations, and quality.
  • Ensure transparent communication across all stakeholders, vendors, CROs, and clinical sites.

Requirements & Qualifications

  • 3 to 8 years of professional experience within a Contract Research Organization (CRO) or related pharmaceutical environment.
  • Bachelor’s degree in Law, Business, Economics, or a closely related field.
  • Strong contract negotiation skills with proven ability to interpret complex legal terminology.
  • Outstanding project management, interpersonal, and diplomatic competencies.
  • Advanced proficiency in standard office software including Excel, Word, and PowerPoint.
  • Familiarity with electronic Trial Master File (eTMF) and contract management systems.
  • Legal authorization and residency to work remotely in eligible European countries.

Required Skills

  • Contract Negotiation & Management
  • Clinical Trial Operations
  • Legal Interpretation & Drafting
  • Project Management & Organization
  • Stakeholder Communication
  • Risk Mitigation & Problem Solving
  • Cross-Cultural Team Collaboration

About Parexel

Parexel is a leading global clinical research organization (CRO) dedicated to accelerating the development of innovative new therapies to improve patient health. By combining expertise across therapeutic areas, advanced technology, and a compassionate, patient-first culture, Parexel empowers biopharmaceutical clients worldwide to achieve clinical success.

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Frequently Asked Questions

Q: What is the role of a Site Contract Lead at Parexel?
A: A Site Contract Lead oversees the complete clinical trial contracting lifecycle, managing strategy, drafting, negotiations, and execution to ensure successful trial delivery.
Q: How many years of experience are required for this position?
A: Candidates are generally required to have between 3 to 8 years of relevant professional experience within a CRO or related pharmaceutical field.
Q: Is this a remote work opportunity?
A: Yes, this role is remote-based, open to candidates residing and authorized to work in specific European countries including Serbia, Poland, Romania, and others.
Q: What educational background is preferred?
A: A Bachelor’s degree in Law, Business, Economics, or a related field is preferred, though equivalent industry experience is also evaluated.
Q: How can I submit my application?
A: You can apply online by visiting the official Parexel career portal through the direct application link provided on JobsCheck.
Q: Are there opportunities for career growth at Parexel?
A: Yes, Parexel offers robust career development programs, continuous learning opportunities, and supportive management to foster long-term professional growth.
Disclaimer: This job post is prepared by collecting data from the official career page of Parexel. We are not direct recruiters or representatives. Candidates should carefully review the requirements and policies on the company’s portal before initiating an application.