PrimeVigilance, part of Ergomed PLC, is a leading global pharmacovigilance service provider dedicated to improving patient lives through expert medical information, regulatory affairs, and safety services. We are currently seeking a Senior Pharmacovigilance Associate to join our international team and contribute to our mission of delivering high-quality safety solutions for our pharmaceutical and biotechnology partners.
Key responsibilities
- Processing Individual Case Safety Reports (ICSRs) from various sources in compliance with global regulations and client-specific requirements.
- Managing SAE/SUSAR processes, including unblinding, clinical trial reconciliation, and protocol reviews.
- Performing MedDRA and WHO coding while ensuring accurate database outputs and reporting.
- Handling product quality complaints and coordinating with Quality Assurance teams.
- Acting as a Local Contact Person for Pharmacovigilance (LCPPV) or Person Responsible for Local Screening (PRLS) as required.
Requirements
- Degree in life sciences, pharmacy, nursing, or a related healthcare field.
- Minimum of 1 year of professional experience in pharmacovigilance.
- Strong organizational skills with a high level of attention to detail and multitasking abilities.
- Advanced proficiency in English, both spoken and written.
- Advanced computer literacy, particularly with the MS Office suite.
What we offer
- Comprehensive training programs and clear pathways for career development.
- A strong emphasis on personal and professional growth within a supportive environment.
- The opportunity to collaborate with a diverse, global team in a human-centric workplace.
- A culture that values well-being, mental health, and a healthy work-life balance.