Safety Specialist – Pharmacovigilance

About the role

Join Thermo Fisher Scientific as a Safety Specialist and contribute to patient safety across global clinical trials. You will perform day‑to‑day pharmacovigilance activities in a highly regulated environment, ensuring accurate collection, assessment, and reporting of safety information.

Key responsibilities

• Collect, code, assess, and enter adverse event data into multiple databases.
• Review cases for quality, consistency, and accuracy, including peer reports.
• Prepare and maintain regulatory safety reports and support audit preparation.
• Collaborate with project teams, investigators, reporters, and third‑party vendors.
• Assist with project implementation, presentations at client/investigator meetings, and budget/metric reviews.

Required profile

• Bachelor’s degree or equivalent with at least 2 years of relevant experience.
• Understanding of pathophysiology, disease processes, and therapeutic areas relevant to the role.
• Strong critical‑thinking, problem‑solving, and communication skills.
• Ability to prioritize tasks, meet strict deadlines, and work with limited supervision.

Required skills

• Proficiency with Microsoft Office suite (Outlook, Word, Excel).
• Experience working with multiple safety databases.
• Good command of English and ability to translate information when required.