Cpl Life Sciences – Regulatory

Principal Regulatory Consultant /Senior Consultant

Location
Letchworth Garden City
Posted
04 May 2021
Closes
02 Jun 2021
Ref
JO-2105-467589
Contact
Charlie Harris
Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
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

Permanent position.

Reference: JO-2105-467589

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.

Responsibilities

-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.

Requirements

-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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