07 ago
|
Thermo Fisher Scientific
|
México
07 ago
Thermo Fisher Scientific
México
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.
📌 Safety Spec (México)
🏢 Thermo Fisher Scientific
📍 México