Safety Data Management

My client is looking for a Safety Data Manager to join an International Drug Safety team in Global Pharmaceutical company (headquarters). As a function within International Clinical Research, the client is responsible for the evaluation and surveillance of all company products, both marketed and in clinical development. Daily work demands good co-operation with cross-organisational departments such as clinical development, registration, quality, and marketing functions in headquarter as well as worldwide affiliates.

Your job
As a Safety Data Manager, you will be responsible for data entry of adverse event reports in English into company’s international safety database including evaluation, coding and follow up on the reports. You will be working within a team and working according to current Standard Operation Procedures. On a daily basis you will communicate with subsidiaries, clinical research personnel and partners to secure timely follow-up on adverse events reported. You will also be involved in tasks like preparation of Periodic safety Update reports and reconciliation between the clinical trial database and the company’s safety database. As a Safety Data Manager you will take part in development and maintenance of the quality system within your area and you will be part of a professional and humoristic working environment.

Qualifications
Ideally from a qualified as a nurse, fluent in English (written and verbal) with knowledge of medical terminology is key. Experience within a similar role is vital and only candidates with a previous background in Safety Data Management will be considered for this opportunity.
This role is an office based role.

For further information please forward your CV details to [Email hidden] or alternatively call Manpreet Mangat on 0044 (0) 207 255 6600