- Implement Regulatory Plan in-line with affiliate business plans
- Ensure Submissions and Approvals for Regulatory Applications in a timely manor.
- Prepare and support new MAAs
- Assist with the maintenance for MAAs
- Interact with Health Authorities
- 6-24+ months experience in Regulatory Affairs
- Experience with submissions to the MHRA is essential
- Bachelor's degree or equivalent in a relevant scientific subject
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Regulatory Affairs Associate - Maidenhead, United Kingdom - Planet Pharma
Description
Role: Regulatory Affairs Associate
Location: Maidenhead / M4 corridor.
Salary: Very competitive salary on offer
Planet Pharma are supporting a leading large global pharma company with the search for a new Regulatory Affairs Associate to join them during an exciting period of growth Perfect for a junior regulatory professional with 6-24 months regulatory experience
Role summary:
Manage the operational and technical aspects of regulatory affairs for the UK, Ireland and Maltese marketing affiliates.
Responsibilities:
Requirements:
If you would like to discuss this vacancy further or to discuss your career options in confidence, please email me on: tcook--
If this role isn't suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated Planet Pharma offers a competitive referral scheme so you will be rewarded for your help
About Planet Pharma
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
