Senior Drug Safety Scientist

The Senior Drug Safety Scientist will be reporting into the Pharmacovigilance manager and will be responsible for:
* Log AE and SAE reports.
* Support the production of PSURs through data retrieval and cleanup activities (including identification of duplicate cases, listedness assessments etc).
* To log and action the processing of ICSR (ASPRs, literature) and spontaneous cases on to the database. This is to be done within agreed timelines and within compliance with SOPs (standard operating procedures) and submitting cases to regulatory authorities.
* Performing duplicate search of the ICSR and spontaneous cases received on Argus database.
* To prioritise, plan, organise work assignments and to work under strict timelines to complete daily tasks/duties.
* Medical Coding of adverse reactions and patient medical history using MedDRA. Drug coding using company and WHO dictionary Assessment of the adverse reactions by looking into company core safety information
* Perform literature searches.
* Responsible for drafting accurate case narrative on to Argus database.
* Participate in team meetings.
* To maintain current working knowledge of company procedures and global drug safety regulations

Experience with Eudravigilance and E2B Reporting is essential.

If you are interested in this role please contact Jessica Warden-Brown and send an up to date CV for consideration.

To find out more about Real Staffing please visit www.realstaffing.com