Clinical Feasibility Analytics Manager

ICON Strategic Solutions; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in the UK seeks a Feasibility Analytics Manager to enhance clinical trial design through data-driven insights and analytics. The role involves close collaboration with global teams to optimize trial execution and operational efficiency, requiring at least 5 years of experience in clinical trial operations and a relevant degree. The company offers a competitive salary along with comprehensive benefits focused on well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Retirement planning benefits

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• At least 5 years of relevant experience in clinical trial execution.
• Expertise in drug development, and clinical trial operations.
• Strong understanding of information systems and statistical principles.

Responsibilities

• Validate and manage standard analytical packages for feasibility.
• Consult on insights for trial operational design and efficiency.
• Drive implementation of feasibility initiatives and technologies.

Skills

Clinical trial execution

Communication skills

Strategic planning

Data-driven approaches

Project management

Education

Bachelor’s Degree in a scientific or health-related discipline

Master’s Degree or higher

Tools

CTMS

Study Optimizer

MS Office (Excel, PowerPoint, Word)

Job description

Feasibility Analytics Manager

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 Feasibility Analytics Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

What you will be doing:

• Provide Standard Analytical Product Package E2E services with regards to feasibility as part of the End to End Process (E2E) within Global Development, aligned with the program level strategy within the agreed timelines and at the highest quality standards. Intelligence services include:
• Ultimately responsible for validating, checking and managing the correct and complete production of standard analytical packages through internal teams and vendor teams
• Consult with Global Feasibility Heads/Leads on insights that should be exemplified and highlighted and connect the data with application to trial operational design and efficiency
• Provide intelligence regarding program planning, protocol design, country and site placement, and enrollment modelling utilizing data-driven approaches to influence optimized approaches to clinical trial execution
• Collect and report on clinical trial performance metrics regarding trial placement, optimization, and enrollment
• Drive the implementation and improvement of Feasibility initiatives/processes/technologies to support and continually evolve standard analytics
• Enable tactics to support the Feasibility Lead in program and protocol planning deliverables such as recruitment rates, site numbers, enrollment estimates, country footprint, startup timelines, impact of protocol criteria, and site and patient profiles
• Function as a System Matter Expert (SME) for operational feasibility systems for internal and external customers
• Track efficiencies resulting from the implementation of new technology initiatives related to program planning, country and site selection, enrollment tracking and protocol optimization
• Effectively partner with CROs to establish and follow operational enrollment technology and operational business processes

You are:

• Bachelor’s Degree is required, preferably in a scientific or health-related discipline. A Master’s Degree, or higher, is preferred
• At least 5 years of relevant experience in clinical trial execution with a pharmaceutical company and/or a CRO
• Expertise in the areas of drug development, clinical trial operations, and strategic planning
• Experience in driving and implementing new technologies
• Excellent communication skills and the innate flexibility to work in a rapidly growing organization
• Strong understanding and experience with information systems (e.g., CTMS, Study Optimizer) and an understanding of basic statistical and epidemiological principles
• Ability to apply data insights to optimize a strategy or scenario
• Strong planning and tracking skills, customer focused, well organized, detail oriented and capable of successfully managing multiple projects
• Excellent time, priority, and self-management capabilities
• Proficient MS Office capabilities (e.g. Excel, PowerPoint and Word)

What ICON can offer you:

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.

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

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.

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 or submit a request here.

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.

Are you a current ICON Employee? Please click here to apply.