Senior Scientist, Pharmacoepidemiology and Safety (UK-based)

Senior Scientist,Pharmacoepidemiology & Safety UK-based Genesis Research Group is one of the leading evidence generation consultancies providing agile, tech-enabled real-world evidence (RWE), as well as health economics and outcomes research (HEOR) solutions to clients in the pharmaceutical, biotech, and medical device industries. Since 2009, we\’ve partnered with our clients to develop impactful evidence across the product lifecycle to optimize market access for novel healthcare innovations and satisfy regulatory, provider, and payer evidence requirements.Genesis is database agnostic, regularly working across many structured and unstructured real-world data sources. As a company, we deliver services across many RWE and HEOR applications and a wide range of therapeutic areas with an emphasis on uncompromising quality, scientific rigor, and flexible solutions.The Genesis Research Group pharmacoepidemiology and safety team consists of scientific experts who lead study design, methodology development, and result interpretation across a broad range of regulatory and safety RWE studies. The individual in this role will demonstrate a passion for the generation of rigorous and relevant RWE, ensuring delivery of high-quality evidence in a timely manner to fully meet our clients\’ needs. This position will report to a Director or Senior Director in Pharmacoepidemiology and Safety.Flexible – hybrid or remote, depending on location.Accountabilities within this role Develop scientifically-sound, clear, concise RWE deliverables related to study design, methodology, and result interpretation (for example: study concept sheets, protocols, analysis results/interpretation, final study reports, slide decks, regulatory briefing books, risk management plans, manuscripts etc.).Contribute effectively to a team of pharmacoepidemiologists, biostatisticians, and analysts charged with designing, implementing, and managing a wide range of studies to assess the utilization, effectiveness, and safety of medicinal products.Collaborate within the organization as it relates to pharmacoepidemiology and safety by supporting cross-functional teams through the design, execution, and delivery of high-priority and high-visibility RWE studies.Ensure best practices with respect to RWD data source selection and research methodology, assessing strengths and limitations when designing studies; appropriately accounting for implications of underlying RWD generation mechanisms and medical coding practices.Cultivate a positive work environment.Qualifications Master\’s degree or PhD within a relevant discipline (e.g., Pharmacoepidemiology or Epidemiology focus on methods and study execution)4+ years for Master\’s degree or 2+ years for PhD of consulting, industry, or academic experienceExperience generating and interpreting real-world and observational researchExperience designing and executing studies using claims and/or EHR databasesStrong regulatory and life sciences industry knowledgeExcellent verbal and written communication skillsProficiency in relevant software such as MS Office (Word, Excel and PowerPoint)Exceptional organizational skills and attention to detailEnthusiasm to learn and motivation to develop oneself and others within Genesis Research GroupFlexibility to adapt to client project needs and handle competing priorities in a fast-paced workplaceCompensation Performance-related bonusFlexible Paid Time OffEmployer matched pension planPrivate Medical InsuranceGenesis Research Group is an equal opportunity employer. Learn more about our values and experience a better way to grow your evidence-based research career.#J-18808-Ljbffr