Regulatory Affairs Manager
Oliver Care at CK Clinical is recruiting for a Regulatory Affairs Manager to join a company in the pharmaceutical industry at their site based in Hertfordshire on a 12 months contract basis.
The main purpose of the role will be:
- Should have experience in standard lifecycle management in particular to Type 1A/B,Type 2 variations and PSUR submission.
- Contributing to the development and implementation of regulatory strategy for own functional teams.
Further responsibilities will include:- Developing an understanding of the importance of lifecycle management and how key regulatory strategies and activities can fulfil commercial needs and maximise assets.
- Compiling regulatory documentation and contributing to the regulatory submission activities.
In order to be considered for this role, you will be required to have the following qualifications, skills and experience: Educated to degree level above in the life sciences or a related field with experience with regulatory methods and processes in an industry setting.
For more information or to apply for this position, please contact Oliver Care on 01438 842976 or email firstname.lastname@example.org. Alternatively please click on the link below to apply online.
CK Clinical is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL33156 in all correspondence.