Description
This role will require the successful candidate to have worked within Regulatory Affairs within a similar Pharmaceutical company or CRO most recently.
Your role will be to understand the current processes in place/understand the documentation already used and Create/Maintain/Archive the regulatory strategies, submissions and other documents within the Trial Master File.
Key Responsibilities include
Provide EU regulatory input to the Regulatory Team and advise early product teams on regulatory strategy with support from piers and managers
Liaise with Clinical Study Teams, Local Offices and CRO partners to facilitate site/study initiation
Manage TMF documents involved with process and procedures across the company
Facilitate and support process change/improvements to projects
Please email an up to date CV for full details.
Allegis Group Limited and Aston Carter Limited operate Employment Businesses and Agencies and are companies within the Allegis Group Inc. group of companies, the fourth largest staffing company in the world, (collectively referred to as the "Allegis Group"). TEKsystems and Aerotek are divisions of Allegis Group Limited. Applicant data will be treated in accordance with the Allegis Group's Privacy Notice.