Clinical Feasibility Informatics Manager

As a Global Feasibility Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Supports to conduct the end-to-end feasibility process
• Prepares and coordinates briefing information, training resources, and other materials.
• Provides project planning support and manage key deliverables.
• Coordinates the feasibility activities on country level Ensures accurate and reliable feasibility data, successful study allocation and planning timelines.
• Coordinate and involve the local GCO and non GCO role (CRMAs) based on their TA and local knowledge and expertise Coordinate and manage the editing, technical support resolution, and distribution of feasibility questionnaires at the trial level between sites, countries, and globally.
• Ensure feedback from feasibility assessments is addressed.
• Conduct scenario planning and provide outputs from Footprint Optimizer (FPO) to assist with timeline review, validation of key data, and support for Final Allocation Curve as part of handover.
• Assist in portfolio management activities, including tracking tollgates and preparing for risk review sessions.
• Draft risk slides and SPF overviews of current feasibility work for senior management.
• Ensure required end-of-feasibility information entry and compliance records into internal systems (e.g., CTMSs forecasting, planning and study deliverables.
• Manage early timeline and pricing assessments, liaising with Health Insights and/or performing competitive intelligence searches to build assumptions (includes archiving outputs in team repositories).
• Manage logistics for team meetings, including agenda preparation, minutes, and follow-up on action items.

You are:

• Bachelor's degree preferred.
• Fluent in English, both written and verbal.
• At least 4-5 years of experience in the end-to-end global feasibility process in clinical trials.
• Experience in creating feasibility dashboards for stakeholders/clients.
• Excellent communication skills.
• Strong project planning and organizational capabilities.
• Proven ability to work independently or in a team setting to meet goals within budget, timeline, and compliance expectations.
• Knowledge of Good Clinical Practice and understanding of the overall drug development process.
• Strong skills in MS Office Suite, including MS Teams, Excel, Word, and expert-level PowerPoint slide creation and formatting.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

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, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.