ICON

Site Contracts Negotiator - Study Start Up

In short

This role manages negotiation and execution of clinical trial agreements and budgets with investigator sites for a global clinical research organisation (CRO). It covers a portfolio of contracts, liaising with legal, finance and project teams, and mentoring junior colleagues. It requires relevant experience in site contracting or contracts administration within CRO, pharma, or healthcare, plus fluency in English and one of French, German, Italian, or Spanish. Based in Sofia, Bulgaria, with office or homebased work options.

Study Start Up Associate - Sofia, Bulgaria - 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 Site Contracts Negotiator II at ICON, you will independently manage the negotiation and execution of clinical trial agreements and budgets for a range of studies. You will work closely with sites and internal stakeholders to support efficient and compliant study start-up.
What You Will Do
You will contribute to contract management activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
•Negotiating site contracts and budgets with investigator sites, within defined parameters and playbooks.
•Reviewing and adapting contract language to reflect sponsor requirements, local laws, and site feedback.
•Managing a portfolio of contracts, monitoring cycle times, and proactively addressing barriers to execution.
•Collaborating with legal, finance, and project teams to resolve contractual questions and ensure alignment.
•Maintaining accurate records of negotiations, approvals, and executed agreements in relevant systems.
•Supporting continuous improvement in contract templates, processes, and guidance, and mentoring junior colleagues where appropriate.
Your Profile
You will bring relevant contract management experience, along with the following qualifications and skills.
Required qualifications and experience:
•Fluent in English and one of the following languages: French, German, Italian, Spanish
•Bachelor's degree in law, business, life sciences, or a related field, or equivalent experience.
•Relevant experience in site contracting, contracts administration, or similar roles within CRO, pharma, or healthcare.
•Good understanding of clinical trial agreements and budget negotiation principles.
•Strong negotiation, communication, and organisational skills.
•Ability to manage multiple contracts and timelines, with attention to detail and quality.
•Proactive, solution-focused mindset with a collaborative approach to stakeholders.
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.

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