Safety Scientist- Real World Evidence (RWE), EMEAVerified as a real position

Who we’re looking for

• 5+ years of experience in data analysis to understand complex linkages of safety data from various sources, preferably in a pharmaceutical, biotech, or healthcare setting.
• Experience working with safety databases required, experience with large healthcare datasets (e.g., EHR, claims, registry data) is a plus
• Proficiency in data extraction from the safety database (e.g. Argus Safety) and generating data insights using adequate digital tools.
• Ability to identify gaps and translate them into actionable plans, especially cross-functionally, through technological tools (e.g. GenAI, Copilot, automation tools, etc.) without compromising clinical integrity.
• Degree in Data Science, Epidemiology, Biostatistics, Public Health, Computer Science, or a related field.
• Familiarity with data visualization tools such as Tableau or Power BI, safety signal tools such as E Empirica, or cloud-based data platforms.
• Proficiency in statistical programming languages (e.g., R, SAS, Python) is a plus.
• Minimum of 5 years working in pharmaceutical/biotech industry.
• Experience in regulated environments (both GCP and GVP).
• Experience in RWE generation, pharmacoepidemiology and/or rare disease is a plus.
• Ability to travel up to 20% of time as needed.

What you’ll do

• As a Safety Scientist III, you will be responsible for the planning, coordination, and delivery of signal detection and product safety scientist activities, with a focus on tasks that are low to high in complexity or which concern low to high complexity products.
• Additionally, you will support the mentoring of more junior colleagues, the development of processes, tools, and systems, and may serve as lead on smaller FSP-type projects.
• Support strategies for safety data generation, assessment, and communications by regular interactions with Safety Evidence Leads and other stakeholders across the organization world-wide, to gather information on topics to be analysed and present findings at internal meetings.
• Synthesize contributions from multiple sources of data into meaningful insights in order to demonstrate product(s) value.
• Monitor competitive environment for new safety information, and compares to safety information of our product(s), thus supporting differentiation activities.
• In collaboration with Safety Evidence Leads and other stakeholders such as Biostatistics and Digital Technology, establish safety evidence information platforms/dashboards and oversees regular updates.
• Identify areas for innovation including AI/machine learning and similar.
• Conduct data mining activities on regular basis to identify data gaps, and communicate safety findings promptly.
• Ensure reproducibility and traceability of analyses through structured workflows and version control.
• Maintain documentation of data extraction and analyses.
• Assist in the design, execution, and reporting of pharmacoepidemiologic studies to address specific safety questions.
• Attends relevant internal and external meetings for training, competitor intelligence, and collaboration with KOLs and other experts.

About the position

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Safety Scientist III – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in patient safety.

Benefits

• When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence.
• You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
• Apply today to help us deliver tomorrow’s breakthroughs.