OverviewLocation / Division Specific InformationThis role offers 100% remote working flexibility in Europe.At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.Work ScheduleEnvironmental Conditions: Office.ResponsibilitiesDesign and implement systematic and targeted literature reviews.Act as principal investigator on indirect treatment comparison (ITC) analysis projects and direct, oversee, and have overall responsibility for all aspects of study design and execution.Provide clients with strategic consultation and advice on how best to address research needs; guide project managers and research associates in delivering required studies.Independently direct key aspects of ITC, SLR, and other literature-based research projects and manage multiple projects.Lead project teams in execution of work; evaluate evidence base to determine feasibility of ITC analyses.Conceptualize advanced study designs and develop study protocols and analysis plans in collaboration with statisticians; oversee ITC analyses and interpret findings.Lead interactions with clients in the pharmaceutical and medical device industries.Manage project budgets, deliverables, timelines; identify scope expansion and need for amendments.Review and finalize project deliverables; ensure study findings are valid and reliable.Support business development, including input into proposal reviews, kick-off meetings and bid defense meetings; review challenges and suggest solutions.Support sales through methodological excellence (SLRs, ITCs, targeted reviews) and review/own annual sales targets.Direct non-billable activities to improve scientific methods, develop internal processes, design proposal approaches, supervise junior staff, and pursue new business opportunities.Serve as consultant to other principal investigators or staff on evidence synthesis tasks; act as guide and mentor across Evidera locations.Travel domestically and internationally occasionally.QualificationsPhD or Master’s in health sciences, economics, biology, natural sciences or related field with 8+ years relevant SLR and ITC experience; or Bachelor’s with extensive relevant SLR and ITC experience.Proven experience in SLR and ITC methods in health economics and/or health services research.Deep understanding of research principles, relevant methodology, and practical research implementation.Specialist skills in population-adjusted indirect comparisons or epidemiology desirable, not required.Experience with HTA/regulatory submissions, including NICE, SMC, and other European HTA bodies and the EMA.Strong organizational skills with ability to oversee multiple projects, meet deadlines, and satisfy client needs.Excellent communication skills, including presentations; competent in written and spoken English.Proficiency with MS Word, PowerPoint, and Excel.BenefitsWe offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
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