Job Description
About the position The Research Scientist position at Thermo Fisher Scientific involves serving as an independent principal investigator and consultant for projects within the Real-World Evidence team. This role is responsible for overseeing project delivery, ensuring scientific integrity, and leading interactions with clients in the pharmaceutical and medical device industries. The position requires a strong background in epidemiology and quantitative methods, with a focus on designing and implementing non-interventional studies. Responsibilities β’ Oversee all aspects of project delivery, including delegating project management tasks to junior staff. β’ Design and implement de novo data collection studies, including retrospective, prospective, and cross-sectional studies. β’ Lead interactions with clients in the pharmaceutical and medical device industries. β’ Review and finalize project deliverables, ensuring validity and reliability of study findings. β’ Manage project budgets, timelines, and scope expansions, identifying the need for amendments. β’ Contribute to abstracts and manuscripts as co-author or first author when possible. β’ Serve as a consultant to other principal investigators or staff on various projects. β’ Guide and mentor staff across Evidera locations. β’ Participate in business development and identify new project opportunities. Requirements β’ PhD in epidemiology or a closely related field, or MSc with 7-10 years of relevant experience. β’ Knowledge of the drug development process and familiarity with international regulatory requirements. β’ Broad experience in quantitative methods in Real World Evidence (RWE) with a focus on non-interventional studies and data analysis. β’ Strong understanding of relevant methodology and statistics. β’ Deep understanding of healthcare research principles and practical research implementation. β’ Working knowledge of MS Office; ability to read and understand SAS/STATA output; familiarity with data analysis software (e.g., SAS, Stata, R) is a plus. Nice-to-haves β’ Experience with the design of peri- or post-approval late phase interventional studies. Benefits β’ Health insurance coverage β’ 401k retirement savings plan β’ Paid holidays β’ Flexible scheduling β’ Professional development opportunities Apply tot his job Apply tot his job