Principal Regulatory Consultant /Senior Consultant
- Experience Level
- Experienced (non-manager)
Principal Regulatory Consultant / Senior Regulatory Consultant
Location: Hertfordshire / Home-based
Salary: Flexible, dependant on experience- includes a car allowance and 15% bonus
CPL Life Sciences are collaborating with a respected scientific regulatory consultancy to hire professionals who have experience working throughout the drug development process. In this role you will work as part of a wider team to support and/or lead regulatory projects presented by innovative clients.
-Support / Lead regulatory submissions, CTA, MAA, amendments, PIPs, scientific advice request, ODD etc.
-Manage / support regulatory procedures at both the national and EU level, supporting US projects
-Support business development activities as required.
-Provide regulatory strategic advice on guidelines, legislation, and procedures to clients on assigned projects.
-Minimum of 8+ years experience working within Regulatory Affair
-Experience working with scientific advice requests, PIPs and Orphan drug applications is highly advantageous
-Good work ethic & strategic mindset
-Relevant life sciences degree
-Experience working with EU requirements, US highly advantageous
If you are interested in this role or would like more details please email your CV to Charlie.harris@CPL.com
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