Contract Analyst

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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

As a Contract Analyst at ICON, you will prepare, negotiate and finalize agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts.

Responsibilities:

• Prepare, negotiate and finalize agreements and budgets related to clinical trials or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts.

• Work with global teams to reviewand analyze contractual terms and conditions. Assess legal and budget risks in conjunction with team support functions. Partner with Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and drive resolution. Escalate as appropriate.

• Analyze investigator fees in relation to fair market value pricing and ensure alignment with regional standards and Sponsor pricing guidelines. Participate in and/or lead approval escalations as appropriate.

• Provide support for negotiations inconfidentiality agreements, informed consent forms and other ancillary contract documents as required.

• Participate in discussions related to the development of site/investigator budgets aligned with fair market value.

• Manage the contract amendment lifecycle.

• Work with the global CCS team as necessary to review and analyze contractual terms to reach resolution. Assess risks of budget and legal provisions in conjunction with members of the CCS team and support functions. Escalate issues as appropriate.

• Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.

• Assume responsibility for all aspects of legal document and metrics tracking.

• Provide support to review, authorize and/or understand aspects of site payments. Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.

Your Profile:

• Previous negotiation of site clinical contracts and budgets required. Demonstrable strength in mentoring others.

• At least 2 years’ experience in legal, CRO, or Sponsor Site Contract & Budget negotiation work.

• Strong analytical, organizational skills. Excellent written and oral communication skills in both English, and where required, local language.

• Proficient in MS Office (especially MS Word and Excel).

• Good interpersonal skills demonstrated as energetic, proactive, customer focused, and independent critical thinker.

• Education (ED): BA/BSc in business, legal or science related field with a strong preference for paralegal or Juris Doctor (JD).

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What ICON can offer you:

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.

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