Feasibility Analytics Manager – Advanced
Posted 2 days ago
Posted 2 days ago
This is a fully remote position, open to applicants in Netherlands.
• Provide analytics for clinical trials and derive insights for feasibility operations and predictive enrollment strategies.
• Identify and implement solutions for disease-specific market assessments, benchmarking, country tiering, site selection, and enrollment modeling.
• Collaborate with FAMs, the Head of Feasibility Analytics, the Feasibility Analytics Innovation team, and Global Feasibility Leads.
• Execute and leverage new technology initiatives related to feasibility and enrollment modeling.
• Work with feasibility and operational databases and technology platforms; gather clinical data, generate insights, discuss findings with feasibility teams, and optimize patient enrollment scenarios.
• Deliver standard analytical product package end-to-end services for feasibility within Global Development.
• Conduct benchmarking, competitive landscape evaluations, country tiering, and site profiling.
• Create enrollment forecasts, assist in plan development, and monitor study enrollment progress using information systems like Monte Carlo Simulations and Study Optimizer.
• Validate, oversee, and manage the complete production of standard analytical packages through internal and external teams.
• Consult with Global Feasibility Heads/Leads and link data insights to trial operational design and efficiency.
• Offer data-driven intelligence for program planning, protocol design, country and site placement, and enrollment modeling.
• Collect and report on clinical trial performance metrics.
• Lead the implementation and enhancement of feasibility initiatives, processes, and technologies.
• Assist Feasibility Leads with recruitment rates, site counts, enrollment projections, country footprint, startup timelines, protocol criteria impact, and site and patient profiles.
• Act as a subject matter expert for operational feasibility systems.
• Monitor efficiencies from technology initiatives related to program planning, country and site selection, enrollment tracking, and protocol optimization.
• Collaborate with CROs on operational enrollment technology and business processes.
• Promote KPIs and optimize practices within therapeutic areas, data analytics, and technologies; escalate technology and vendor issues when necessary.
• Coordinate with Feasibility Data Sciences to develop data-generated insights and visualizations.
• Engage in Global Development initiatives and assigned system projects.
• Establish methodologies for data analytics to derive operational and feasibility insights.
• Train and develop other FAMs in new technologies and methodologies.
• Establish thought leadership in feasibility analytics.
• Participate in projects involving Feasibility Data Scientists and drive innovation.
• A Bachelor’s Degree is mandatory, preferably in a scientific or health-related field.
• Minimum of 5 years of relevant experience in clinical trial execution within a pharmaceutical company and/or a CRO.
• Proficiency in drug development, clinical trial operations, and strategic planning.
• Experience in Oncology or Cross Therapeutic Areas; Oncology experience is advantageous.
• Proven track record in driving and implementing new technologies.
• Excellent communication skills and adaptability to work in a fast-paced, growing organization.
• Strong familiarity and experience with information systems such as CTMS and Study Optimizer.
• Basic understanding of statistical and epidemiological principles.
• Ability to leverage data insights to refine a strategy or scenario.
• Exceptional planning and tracking abilities; customer-focused, organized, detail-oriented, and capable of managing multiple projects.
• Strong capabilities in time management, prioritization, and self-management.
• Proficient in MS Office applications, including Excel, PowerPoint, and Word.
• Experience in statistical analysis and analytical models, particularly in enrollment modeling, simulation, and forecasting.
• Strong understanding of clinical trial operations data.
• Advanced skills in MS Office, Tableau, or other visualization software.
• Effective leadership skills with a proven ability to enhance team productivity and cohesion.
• Legal eligibility to work in the country where the position is based.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career pathways.
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