Drug Safety Specialist – Night Shift

About the role

Join a leading pharmacovigilance team and help ensure patient safety across global clinical trials. As a Drug Safety Specialist working night shifts, you will perform day‑to‑day PV activities in a highly regulated environment, supporting both internal teams and external partners.

Key responsibilities

• Perform daily PV tasks including data entry, adverse event coding, case review, follow‑up, and regulatory safety reporting.
• Participate in on‑call duties to provide 24‑hour coverage for case intake from investigative sites.
• Review pharmacovigilance publications and regulatory updates to stay current on guidelines.
• Maintain medical knowledge of therapeutic areas and disease states relevant to the projects.
• Prepare and maintain regulatory safety reports and assist with project implementation, presentations, and audit preparation.
• Mentor junior staff and contribute to the development of departmental procedures.

Required profile

• Bachelor’s degree or equivalent in a relevant field.
• At least 2 years of experience in pharmacovigilance or related safety monitoring.
• Strong understanding of pathophysiology and disease processes.
• Excellent critical thinking, problem‑solving, and written/oral communication skills in English.
• Ability to translate safety information into local languages when required.
• Computer literate with proficiency in handling multiple databases and PV tools.

Required skills

• Data entry
• Adverse event coding
• Regulatory safety reporting
• Computer literacy

What we offer

• Opportunity to work on high‑impact clinical trials for top pharmaceutical companies.
• Collaborative office environment with experienced PV professionals.
• Professional development and mentorship programs.