A global pharmaceutical company is looking for a pharmacovigilance professional to join their team on a permanent basis in Oxfordshire.
- To ensure that all medical writing documents prepared for assigned Clinical Research Programs within R&D are prepared in accordance within rigorous, objective and informative medical writing procedures and processes.
- To lead the Medical Writing activities for US, European or other regulatory submissions as assigned.
- To ensure documents for assigned clinical trials are prepared, reviewed, and approved in a quality, timely and accurate manner such that the data presented will withstand examination by regulatory bodies.
- To support the full use of the Electronic Document Management System (EDMS) for all assigned products within the company.
If you have experience in Medical Writing and open to a new opportunity, don't hesistate to get in touch,
To find out more about Real please visit www.realstaffing.com
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales