Senior Site Contracts Negotiator

Posted 2 Days Ago
Be an Early Applicant
2 Locations
In-Office or Remote
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Leads negotiation and management of clinical trial site contracts and budgets across multiple countries. Reviews terms for legal, regulatory, sponsor, and policy alignment; partners with legal, finance, and project teams; resolves site issues; monitors cycle times; and improves templates, playbooks, and negotiation processes.
Summary Generated by Built In
Senior Site Contracts Negotiator - Slovakia, Czechia, Romania - office or homebased

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 Senior Site Contracts Negotiator at ICON, you will lead the negotiation of clinical trial agreements and budgets with investigator sites, ensuring timely, compliant, and mutually beneficial outcomes.


What You Will Do:

You will lead on contract management tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Leading the negotiation of site contracts and budgets for complex or high-priority clinical studies across multiple countries.
  • Reviewing contract terms to ensure alignment with sponsor requirements, internal policies, and applicable laws and regulations.
  • Serving as a key point of contact for sites on contractual matters, addressing questions and resolving issues in a timely manner.
  • Collaborating with legal, finance, and project teams to ensure consistency of contractual language and budget assumptions.
  • Monitoring contract cycle times and providing input into strategies to reduce timelines and improve efficiency.
  • Supporting the development and refinement of contract templates, playbooks, and negotiation guidelines.

Your Profile:

You will have a strong foundation in contract management, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in law, business, life sciences, or a related field, or equivalent experience.
  • Significant experience in site contracting or clinical vendor contracting within CRO, pharma, or a related industry.
  • Strong understanding of clinical trial agreements, budget structures, and key legal and compliance considerations.
  • Excellent negotiation and communication skills, with the ability to balance site, sponsor, and organisational needs.
  • Fluent in English and Czech
  • Highly organised and detail-oriented, with experience managing multiple contracts and timelines across countries.
  • Solution-focused mindset, with the ability to manage escalation situations and contribute to process improvements.

#LI-DK2

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


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


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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

Skills Required

  • Bachelor's degree in law, business, life sciences, or a related field, or equivalent experience
  • Significant experience in site contracting or clinical vendor contracting within a CRO, pharmaceutical, or related industry
  • Strong understanding of clinical trial agreements, budget structures, and key legal and compliance considerations
  • Excellent negotiation and communication skills
  • Fluency in English and Czech
  • Strong organizational and attention-to-detail skills, including experience managing multiple contracts and timelines across countries
  • Solution-focused approach, including the ability to manage escalations and contribute to process improvements

ICON plc Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.

  • Healthcare Strength — Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
  • Leave & Time Off Breadth — Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
  • Retirement Support — Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.

ICON plc Insights

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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