Safety Spec

Thermo Fisher Scientific

Not Specified, United States Full-time in Other
    • Job ID 1492279

    Job Description

    Job Description

    • Performs day-to-day Pharmacovigilance (PV) activities within a highly regulated environment and driven by strict timelines. PV activities include but are not limited to collection, monitoring, assessment, evaluation, research and tracking of safety information.

    • Coordinates and performs PV activities such as data entry, coding and assessment of adverse events, case review, follow-up, tracking of reports, and regulatory reporting activities.

    • Collaborates, effectively, with various parties such as: project team members, client contacts, investigators, and adverse event/ reporters, and third party vendors.

    • May assist in the preparation of departmental and project-specific procedures and processes, prepare for and attend audits, kick-off and investigator meetings.

    Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

    Other jobs you may like