Regulatory Associate
- Weybridge, ENG (GBR)
- Negotiable
- 6 Months
- Start date: ASAP
- Ref: GSK0JP00075862
- documentation
- Pharma - Regulatory Affairs
Job description
Posted 13 February 2019
Description
Preparation of high quality, detailed regulatory documents using varied information sources.
Liaising closely with other GSK personnel to ensure the accuracy of such records.
Working to agreed deadlines and maintaining records reflecting project status.
Responsible for highlighting potential delaying factors promptly to line management and sharing knowledge of regulatory documentation and procedures with others to assist in problem-solving.
Additional information about the process
All profiles will be reviewed against the required skills and experience. Due to the high number of applications, we will only be able to respond to successful applicants in the first instance. We thank you for your interest and the time taken to apply.a
