
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
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10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
• Design and execute Epidemiology studies addressing safety research questions. • Identify epidemiological / pharmaco-epidemiological methods, relevant data sources, best suited to address safety research questions. • Conduct the feasibility, designing, preparing study concepts, protocols, and statistical analysis plans, and report of pharmacoepidemiologic studies. • Transfer epidemiologic expertise and deliverables to the evaluation, refinement and contextualization of safety findings. • Utilize analytical methods to interpret real world data, support the identification of safety data gaps in order to generate relevant insights. • Contribute to the development of Integrated Evidence Generation Plans (IEGPs), including the planning, prioritization, and execution of real-world studies, with particular focus on safety aspects and outcomes. • Communicate safety RWD internally and externally promptly with all relevant stakeholders. • Collaborate with Scientific Communications on integrated publication plans for safety evidence. • Foster a continuous learning/improvement.
• Background in health and life sciences (epidemiology, public health, MD, pharm D), or quantitative data sciences, biostatistics • PhD in Epidemiology and/or pharmacoepidemiology or equivalent advantageous • 12+ years of experience in epidemiology/ pharmacoepidemiology as well as in drug safety • Excellent written and oral communication skills in English • Strong medical/scientific background, inspired by prioritizing patient safety. • Good working knowledge of both GCP and GVP. • Substantial prior experience of working with RWE/D within the pharmaceutical industry, particularly in the application of RWE in drug development for rare indications is a plus. • Ability to travel up to 20% of time as needed.
• Competitive salary • Flexible working hours • Professional development opportunities
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