Drug Safety Specialist
25.00-30.00 Hourly Rate
We would like to present to you a hugely exciting contract opportunity for one of our global clients who are nestled within the Oxfordshire boarders.
We are searching for a Drug Safety Specialist to join their exisiting, expanding and rewarding team on a contractual basis for a period of 6 months initially.
The Drug Safety Specialist is responsible for participating in the collection, safety review, processing and reporting of adverse event data in compliance with applicable FDA and global regulations and our clients Pharmaceuticals standard operating procedures and guidelines.
Duties will include the following but not limited too:
Perform accurate computer data entry of identified adverse event information and ensure the uniform and timely processing and reporting of adverse events to regulatory authorities. The Drug Safety Specialist will assist with Deviation and Notice of Event (NOE) documentation and investigation, where necessary.
The Drug Safety Specialist will participate in the set-up and maintenance of adverse event workflow, and be accountable for the development of department policies and standard operating procedures.
- In addition, the Drug Safety Specialist may contribute to the department relationship with internal and external business partners to meet global regulatory reporting requirements and support other funtions within the Pharmaceutical business areas.
We are looking to offer candidates a very competitive hourly rate and the opportunity to work within a superb team.
If you feel that this may be of interest to you, please get in touch with Kathryn Taylor
Posted 13 days ago