Job Description
Job Title: Regulatory Affairs Consultant
Location: Maidenhead
Contract: 12 months / hybrid 3 days onsite
Hours: 37.5 per week
Rates: £50-60p/h
Job Description
SRG are looking for a regulatory affairs consultant to join a leading pharmaceutical company based in maidenhead. As part of this role, you will be Supporting lifecycle management of applicable products or submissions, management of paediatric investigation plans and clinical trial activities with the Medicines and Healthcare Products Regulatory Agency (MHRA).
Duties and Responsibilities
Overall responsibilities
With supervision and guidance from Line Manager;
- Acts as the primary Regulatory contact for identified portfolio.
- Develops robust regulatory strategies and timelines for those pro...
Ready to Apply?
Take the next step in your AI career. Submit your application to SRG today.
Submit Application