Regulatory Associate - London, United Kingdom - Proclinical Staffing

Description

Proclinical is seeking a Regulatory CMC Associate for a 12-month contract role.

This position will provide support to the Chemistry, Manufacturing and Controls (CMC) function, which is responsible for Module 3 of regulatory submissions across various phases of product development, from clinical to lifecycle.

The role involves organising, managing, and executing regulatory CMC projects and submissions, and may include tasks such as creating and maintaining submission timelines, formatting documents, scheduling meetings, and managing document reviews.

Provide support to the CMC function in regulatory submissions.
Organise, manage, and execute on regulatory CMC projects and submissions.
Create and maintain submission timelines and tables of contents.
Proficiency in Microsoft Office suite, especially Word, Excel, PowerPoint, and Project.
Experience in the biopharmaceutical or pharmaceutical industry (preferred).

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Regulatory