Job Title:
Pharmacovigilance Specialist
About the Role:
We are seeking a dedicated and detail-oriented Pharmacovigilance Specialist to join our team on a permanent full-time contract.
The ideal candidate will have a strong background in pharmacovigilance, quality management systems, and excellent communication skills.
The key responsibilities of this role include case processing, timely reporting of ICSRs, screening of local and global literature for ICSRs, and conducting periodic case reconciliations with clients and business partners.
The successful candidate will also be responsible for drafting PVAs and SDEAs, assisting with GVP inspection readiness activities, and supporting the company during client audits and authority inspections.
Additionally, they will assist with the preparation of signal detection reports, RMPs, PSURs, and PSMFs, as well as continuous improvement of SOPs.
Required Skills and Qualifications:
* Bachelor's degree in Science, Pharmacy, Pharmacology, Nursing, or related discipline
* Minimum 2 years' experience working within pharmacovigilance and quality management systems and procedures
* Commercial awareness and ability to assess commercial implications of decisions and advice
* Awareness and understanding of Pharmacovigilance legislation in Europe and the UK
* Good project management skills with a systematic approach to tasks
* Ability to keep meticulous records and strong attention to detail
* Strong interpersonal and communication skills with proven ability to influence people
* Motivated self-starter with the ability to work independently
About Us:
We offer a challenging and rewarding career opportunity for a motivated and detail-oriented individual looking for a career in pharmacovigilance.
Contact Information:
Please submit your application for this exciting opportunity to progress your career in pharmacovigilance.