Feasibility Analytics Manager – Advanced

🔥 2 minutes ago

🇳🇱 Netherlands – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

📉 Data Analyst

👻 Ghost score 10%

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Deliver clinical trial analytics and generate insights for feasibility operations and predictive trial enrollment • Identify and deliver solutions for disease-specific market analysis, benchmarking, country tiering, site selection, and enrollment modelling • Collaborate with FAMs, the Feasibility Analytics Head, Feasibility Analytics Innovation team, and Global Feasibility Leads • Implement and utilize new technology initiatives related to feasibility and enrollment modelling • Work with feasibility and operational databases and technology platforms; collect clinical data, generate insights, review findings with feasibility teams, and optimize patient enrollment scenarios • Provide standard analytical product package E2E services for feasibility within Global Development • Perform benchmarking, competitive landscape analysis, country tiering, and site profiling • Create enrollment projections, facilitate plan building, and track study enrollment progress using information systems such as Monte Carlo Simulations and Study Optimizer • Validate, check, and manage complete production of standard analytical packages through internal and vendor teams • Consult with Global Feasibility Heads/Leads and connect data insights to trial operational design and efficiency • Provide data-driven intelligence for program planning, protocol design, country and site placement, and enrollment modelling • Collect and report clinical trial performance metrics • Drive implementation and improvement of feasibility initiatives, processes, and technologies • Support Feasibility Leads with recruitment rates, site numbers, enrollment estimates, country footprint, startup timelines, protocol criteria impact, and site and patient profiles • Serve as a subject matter expert for operational feasibility systems • Track efficiencies from technology initiatives related to program planning, country and site selection, enrollment tracking, and protocol optimization • Partner with CROs on operational enrollment technology and business processes • Promote KPIs and optimizing practices within therapeutic areas, data analytics, and technologies; escalate technology and vendor issues as needed • Coordinate with Feasibility Data Sciences to create data-generated insights and visualizations • Participate in Global Development initiatives and assigned system projects • Establish data analytics methodologies for operational and feasibility insights • Develop and train other FAMs in new technologies and methodologies • Establish thought leadership in feasibility analytics • Participate in Feasibility Data Scientist projects and drive innovation

🎯 Requirements

• Bachelor’s Degree is required, preferably in a scientific or health-related discipline • At least 5 years of relevant experience in clinical trial execution with a pharmaceutical company and/or a CRO • Expertise in drug development, clinical trial operations, and strategic planning • Oncology/Cross Therapeutic Area experience; Oncology is a plus • Experience in driving and implementing new technologies • Excellent communication skills and flexibility to work in a rapidly growing organization • Strong understanding and experience with information systems such as CTMS and Study Optimizer • 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 managing multiple projects • Excellent time, priority, and self-management capabilities • Proficient MS Office capabilities, including Excel, PowerPoint, and Word • Experience in statistical analysis and analytical models, especially enrollment modelling, simulation, and forecasting • Strong understanding of clinical trial operations data • Advanced skills in MS Office, Tableau, or other visualization software • Effective leadership skills and proven ability to foster team productivity and cohesiveness • Legal right to work in the country where the role is based

🏖️ 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