Senior Pharmacovigilance Associate

Capital Pharma
13 Nov 2017
16 Nov 2017
Contract Type
Full Time
My client is a UK based consultancy who specialises in Post Market drug safety. They are well renowned for their fantastic training and will provide you with the best support for progressing through your career. Due to growth they are currently looking for a Senior Pharmacovigilance Associate to come and join their office based in Surrey.

Some of the responsibilities included within the role:

- MedDRA coding.
- Literature review.
- Case processing including data entry, narrative writing, review and assessment of SAE/AE reports from all sources
- Case submissions to regulatory authorities.
- SAE reconciliation.
- Safety data retrieval, supporting information requests production of data for aggregate reports
- Using and maintaining the global safety database.

Senior Pharmacovigilance Associate Level/ What they are looking for:

- 2+ years' experience(variable; candidates with more/less experience welcome to apply)
- Full lifecycle case processing knowledge (data entry and review stages)
- Argus experience
- Knowledge of EudraVigilance
- EVMPD data entry experience
- Narrative writing
- MedDRA coding
- Literature review
- Triage
- Mentoring
- Audit/inspection participation
- Face to face client experience
- PSMF maintenance
- Knowledge beyond local affiliate level
- MI experience

This role would suit either a current Senior Pharmacovigilance Associate or someone wanting to pursue a new challenge or a looking to take a step up within pharmacovigilance (senior level) in a company that can support training and progression.