Pharmacovigilance Associate (Contract)

Role overview

An innovative biotech company is looking for a Pharmacovigilance Associate to support routine drug safety operations on a contract basis. This position is suited to someone with early-stage experience in pharmacovigilance who wants to deepen their knowledge of case handling, safety systems, and regulatory compliance in a dynamic environment.

Assignment details

• Contract duration: 6 months, with the possibility of an extension or conversion to a full-time role.
• Work schedule: 40 hours per week.
• Work mode: Remote.

Key responsibilities

• Handle adverse event case processing and participate in quality review checks.
• Support safety data management activities and reconciliation tasks.
• Work with internal teams and external collaborators to keep safety operations running smoothly.
• Help with inspection readiness efforts and ongoing process enhancements.

Required experience and knowledge

• 1 to 3 years of experience in pharmacovigilance or drug safety.
• Strong preference for candidates with a PharmD.
• Practical exposure to ICSR case processing and quality control review.
• Experience using safety databases and managing the full case lifecycle, from intake through submission or distribution.
• Ability to support case follow-up and maintain data quality throughout the workflow.
• Working understanding of global pharmacovigilance regulations and guidelines, including ICH E2A, E2B(R3), and E2D, as well as FDA and EMA reporting concepts.
• Familiarity with pharmacovigilance SOPs.
• Knowledge of medical coding practices and safety data quality standards.

Additional information

This opportunity is intended for a candidate who can contribute effectively in a fast-moving biotech setting and grow within drug safety operations.

Application note

The hiring team invites interested candidates to get in touch directly for more details.