Site Contracts Negotiator II (German speaker)

Posted Yesterday
Be an Early Applicant
3 Locations
In-Office
Entry level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Independently negotiates and executes clinical trial site contracts and budgets, reviews contract language, manages contract portfolios and timelines, resolves issues with legal, finance, and project teams, maintains negotiation records, improves contracting processes, and mentors junior colleagues. Requires German and English fluency, contract management experience in CRO, pharmaceutical, or healthcare settings, and knowledge of clinical trial agreements and budget negotiations.
Summary Generated by Built In
Site Contracts Negotiator II (German speaker)

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:

  • Bachelor's degree in law, business, life sciences, or a related field, or equivalent experience.
  • Fluency in German and English
  • 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.

#LI-JJ1


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
  • Fluency in German and English
  • Relevant experience in site contracting, contracts administration, or similar roles within a CRO, pharmaceutical, or healthcare organization
  • Understanding of clinical trial agreements and budget negotiation principles
  • Strong negotiation, communication, and organizational skills
  • Ability to manage multiple contracts and timelines with attention to detail and quality
  • Proactive, solution-focused mindset and collaborative stakeholder approach
  • Legal right to work in the country where the role is based

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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