Senior Manager, Contracts

Senior Manager, Contracts

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

What You Will Do:

• Contracts and budget strategy and oversight: Set up and lead the end-to-end operational strategy for study contracting and budgeting across assigned studies and programs, aligning with CSP, country requirements, biosampling plans, and funding envelopes. Serve as the single point of accountability for budget integrity and contract alignment from concept to closeout.-to-end operational strategy for study contracting and budgeting across assigned studies and programs, aligning with CSP, country requirements, -out.

• FMV governance and application: Ensure country level FMV benchmarks are established, current, and consistently applied across study and country budgets, including sites, central/specialty labs, and other vendors. Document FMV methodologies, justifications, and deviations in accordance with compliance and regulations.-level FMV benchmarks are established, current, and consistently applied across study and country budgets, including sites, central/specialty labs, and other vendors. Document FMV methodologies, justifications, and deviations in accordance with compliance and anti-kickback regulations.

• Master study and country budgets and CSA templates: Build, maintain, and own the master study and country budget and CSA templates; perform scenario modelling and sensitivity analysis based on study design changes, enrolment dynamics, and operational assumptions.

• Budget and CSA distribution to countries: Finalize and distribute approved country budgets to SMM/country teams with clear negotiation guidance, parameters, and change control rules. Track implementation and provide clarification during site negotiations as needed. Maintains country study templates and adjusting changes in due course of the study as needed.

• CSA subject matter expertise: Act as portfolio SME and primary POC for Clinical Study Agreements (CSAs) with SMM and Legal. Guide terms, rate structures, study specific appendices, and change orders; coordinate review cycles and approvals to meet startup timelines.-specific appendices, and change orders; coordinate review cycles and approvals to meet start-up timelines.

• Protocol amendment impact assessment: Lead ongoing and ad hoc CSA and budget reviews triggered by protocol amendments or operational changes. Quantify impacts, secure approvals, adjust master and country budgets, and execute contract amendments in a timely and compliant manner.

• Documentation ownership and repository management: Ensure timely maintenance and distribution of contracting documentation, including a complete, version controlled repository of signed CSAs, amendments, rate cards, and budget approvals across the portfolio; ensure eTMF completeness and inspection readiness.-controlled repository of signed CSAs, amendments, rate cards, and budget approvals across the portfolio; ensure eTMF completeness and inspection readiness.

• Partner with Finance on forecasting, risk/opportunity management, and governance reporting, if needed.

• Cross-functional leadership and collaboration: Coordinate deliverables across Study Teams, SMM, Legal, Procurement, Finance, and scientific functions; facilitate decision making, resolve issues, and drive alignment on budget and contract priorities and timelines.-functional leadership and collaboration-making, resolve issues, and drive alignment on budget and contract priorities and timelines.

• Process improvement and standardization: Establish and refine standards, templates, guidance, and tools for budgets and CSAs; identify opportunities for automation and AI enabled solutions; lead or contribute to continuous improvement and change initiatives impacting contracting and budgeting operations.-enabled solutions; lead or contribute to continuous improvement and change initiatives impacting contracting and budgeting operations.

Your Profile:

• University degree (or equivalent), preferably in medical or biological sciences or a discipline associated with clinical research.

• At least 5 years of relevant clinical experience in the pharmaceutical industry focused in Budgets/Contracts, including 2 years of operational strategy experience

• Extensive knowledge of clinical research regulatory requirements; excellent understanding of ICH/GCP, and study management processes, including contracting and study budget management.

• Strong leadership and cross-functional collaboration skills with demonstrated ability to influence without authority and coordinate complex workstreams across scientific and operational functions.

• Proven project management skills, including planning, risk management, timeline and budget oversight; proficiency with standard project tools and IT systems.

• Excellent communication, stakeholder management, and relationship-building skills; strong negotiation and conflict management capabilities.

• Strong organizational and problem-solving skills; ability to manage competing priorities and maintain attention to detail.

• Fluent verbal and written English.

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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