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About the Role

Serve as a technical feasibility strategy expert, leading and managing the process of clinical project feasibility in support of proposal teams. Assist Business Development with cost proposals, provide input on operational strategy, and support client interactions and strategic partnerships.

Responsibilities

• Recognize, exemplify, and adhere to ICON's values (Collaboration, Integrity, Inclusion, and Agility).
• Create a culture of process improvement focused on streamlining processes, adding value, and meeting client needs.
• Participate in sharing FIM learning across therapeutic teams to improve strategic feasibility support and outputs.
• Maintain communication and relationships between all relevant parties to ensure optimal, data-driven feasibility strategy solutions.
• Collect data from data assets, country associates, site level Investigators, and KOL interviews.
• Determine site profiles.
• Develop appropriate feasibility strategies, including approach and management for standalone feasibilities.
• Provide full documentation in the proposal, including incidence/prevalence, treatment practices, reimbursement practices, competitive landscape, and enrollment trend analysis.
• Collaborate with Patient Recruitment, Start-up, and other teams.
• Ensure feasibility data is fully evaluated to determine risks to project delivery and that identified risks are escalated with planned solutions.
• Transition pre-award generated data and strategy to the Site ID Manager/Lead upon award.
• Prepare internal project information to support ad hoc requests.
• Establish project viability through interrogation of internal and external performance metrics and resources.
• Ensure all collected data is high-quality, accurate, and fully documented in ICON feasibility business systems.
• Perform accurate and correct data analysis and interpretation to support feasibility strategy solutions.
• Support and/or present strategic project planning for bid defense meetings.
• Initiate, conduct, coordinate, analyze, and report feasibility studies as contracted on time and on budget.
• Meet Sponsor objectives and expectations.
• Coordinate with the Site ID Lead per RACI.
• Develop appropriate country and site selection strategies and analyze/interpret results to provide protocol feedback and recommendations.
• Document and track feasibility study results.

Requirements

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

Work Type

• Travel (approximately 20%) domestic and/or international as needed.

Experience Level

• 6-9 years of experience in a Clinical Research environment

Education Level

• Master's Degree

Benefits

• 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

About the Company

• 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.

Equal Opportunity

• 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.