Pharmacovigilance Operations Specialist with German

We are recruiting for our global client operating in the clinical research and healthcare data analytics sector. The company partners with leading pharmaceutical and biotech organizations to enhance drug safety and advance patient outcomes worldwide. It offers an international, dynamic, and collaborative work environment where you can develop your expertise and contribute to improving healthcare quality on a global scale.

• Review, assess, and process safety data and adverse event (AE) reports in compliance with applicable regulations, internal SOPs, and project-specific requirements
• Maintain accurate and complete case documentation within pharmacovigilance databases
• Code medical terms and products, prepare case narratives, and perform literature surveillance activities as required
• Ensure high-quality deliverables and adherence to timelines and productivity targets
• Collaborate with cross-functional teams (clinical operations, data management, medical monitors) to resolve safety queries
• Participate in audits and inspections, ensuring full compliance with internal and client quality standards

• Employment contract for 12 months (replacement period)
• Fully remote position – work from anywhere in Poland
• Competitive salary aligned with market standards
• Full onboarding and ongoing professional training
• Opportunities for career growth in an international, knowledge-driven environment

• remote work opportunities

Join our client’s global pharmacovigilance team and play a vital role in ensuring patient safety and regulatory compliance worldwide.

If you are passionate about science, quality, and healthcare innovation – apply today!

Please submit your CV in English.

Manpower