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Site Contracts Lead

Remote, Poland, Warsaw·Added 2 months ago (last checked 19 Oct)

ICON plc

63 open roles

Overview

Work mode
Remote (Poland, Warsaw)
Contract
Permanent contract
English
Required
Benefits
Private health insurance, life insurance, gym access

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Skills

The role

Site Contracts Lead - Home or office based

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Site Contracts Lead at ICON, you will oversee and coordinate the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies or portfolios.

What You Will Do

You will oversee contract management workstreams, ensuring deliverables meet quality and timeline expectations.

Key responsibilities include:

  • Managing end-to-end site contracting activities for assigned studies, including template use, negotiation, and execution tracking.
  • Serving as a primary escalation point for contract issues, proposing solutions that balance sponsor, site, and internal requirements.
  • Collaborating with legal, finance, and project teams to ensure alignment on contract language, budget assumptions, and risk positions.
  • Monitoring contracting timelines and metrics, identifying bottlenecks, and driving corrective actions to improve cycle times.
  • Providing guidance and oversight to Site Contracts Negotiators working on the same studies or programmes.
  • Contributing to the development and refinement of contracting playbooks, templates, and standard processes.

Your Profile

You will have solid contract management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in law, business, life sciences, or a related field, or equivalent experience.
  • Strong experience in clinical site contracting or similar contract negotiation roles within CRO, pharma, or healthcare.
  • Good understanding of clinical trial agreements, budget structures, and key legal and compliance considerations.
  • Excellent negotiation, communication, and problem-solving skills.
  • Organised and detail-oriented, with the ability to manage multiple studies and priorities.
  • Collaborative mindset with experience guiding or coordinating the work of others.

What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family's needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

About ICON plc

ICON is a clinical research organisation (CRO) providing outsourced clinical development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company describes itself as the world's leading clinical research organisation and operates at global scale, with employees in 119 locations across 53 countries.

Its services span clinical and scientific operations, decentralised clinical trials, early clinical and laboratory services, medical imaging, regulatory affairs, consulting, commercialisation, medical writing, biometrics and outcome measures. ICON works across sectors including pharmaceuticals, biotech, medical devices and government and public health, and across therapeutic areas such as oncology, cardiovascular, central nervous system, vaccines and rare and orphan diseases.

Industry
Clinical research
Headquarters
Dublin, Ireland
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