Drug Safety Specialist (Night Shift)

About the role

We are looking for a Drug Safety Specialist to join our pharmacovigilance team on a night‑shift schedule. In this role you will support the safety monitoring of clinical trial participants and ensure compliance with global regulatory requirements.

Key responsibilities

• Perform day‑to‑day pharmacovigilance activities including case entry, coding, assessment, follow‑up and tracking of adverse events.
• Prepare and submit regulatory safety reports and maintain accurate safety databases.
• Review case quality for consistency and accuracy, including peer‑report verification.
• Collaborate with project teams, investigators, reporters and third‑party vendors to gather safety information.
• Participate in on‑call duties to provide 24‑hour case intake coverage.
• Assist in the preparation of departmental procedures, audit readiness and attend client or investigator meetings.

Required profile

• Bachelor’s degree or equivalent in a relevant scientific field.
• Minimum of 2 years of experience in pharmacovigilance or related safety monitoring.
• Understanding of pathophysiology and therapeutic areas relevant to adverse event processing.
• Strong critical‑thinking and problem‑solving abilities.
• Excellent oral and written English communication skills.

Required skills

• Pharmacovigilance (PV) activities and adverse event case management.
• Adverse event coding and regulatory safety report preparation.
• Medical literature review and safety data assessment.
• Computer literacy with ability to work across multiple safety databases and software tools.