This is a fully remote position, open to applicants in Serbia.

📋 Description

• Plan, prepare, conduct, report, and follow up on various types of Pharmacovigilance audits.

• Develop and monitor CAPA plans.

• Execute audits in accordance with regulatory requirements and Good Pharmacovigilance Practice (GVP).

• Carry out GVP quality assurance projects for pharmaceutical and biotechnology client companies.

• Perform both onsite and remote audits throughout Europe.

⛳️ Requirements

• Proven experience in conducting and leading internal and external Pharmacovigilance audits for diverse stakeholders.

• In-depth knowledge of national and international Pharmacovigilance legislation and guidelines.

• Skilled in project management with a focus on timely deliverables.

• Capability to identify issues and provide pragmatic solutions.

• Bachelor’s Degree in Life Sciences is preferred.

• Travel will be necessary for audits, along with conducting remote audits.

🏝️ Benefits

• Full-time or part-time freelance engagement (0.6+ FTE considered).

• Options for remote work.

• Opportunities for professional development.

• Supportive and collaborative work environment.

• Chance to make a significant impact in the pharmaceutical and biotechnology sectors.

• A diverse and inclusive workplace.

• Collaboration with experts in clinical research, pharmacovigilance, and quality consulting.