The Role:Responsible for the coordination of all First Registrations, Renewals, Tenders, Response to questions and Site Registrations submissions. Ensuring delivery to agreed timelines and in...
Liaise with regulatory authorities for advice and guidance when necessary, and to resolve issues to achieve the best possible outcome for the business.
Ensure all processes are carried out according to guidelines and standard operating procedures.
Gap analysis of regulatory documentation, identification of potential challenges and propose solutions.
Managing external pharmacovigilance and medical information agent.
Build and maintain effective relationships with external clients/ partners alongside partner's regulatory teams.
Managing/supporting a range of changing project demands.
Bachelor's degree equivalent or higher qualification within Pharmaceutical or relevant life science.
Extensive experience in regulatory affairs.
Experience working with government agencies and trade organisations to clarify and resolve regulatory matters.
Hands on experience within MENA regulatory submissions.
Ability to work in a stand alone function.
If you are interested in this role or would like to have a confidential career discussion regarding other Regulatory Opportunities. Please contact me: or +441753 589673
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.