The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
General
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.
This well-known biopharmaceutical company is looking for a Regulatory Affairs Labelling Associate Project Manager to join their Labelling team on a contracting basis.
Your new company.
This is a 12-month contract job with scope for extension and is fully remote.
Global Regulatory Affairs - Due Diligence Manager / Senior Manager
This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a 6 month contract but has scope for extension.
Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in UK & Ireland.
Support the Regulatory team with specific tasks per the needs of the department, which may include claims tracker updates, databases, compliance tasks.
Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland.
The ideal candidate will be a diligent and detail-oriented Health and Safety Administrator, and will be responsible for ensuring compliance with health and safety regulations and protocols within the operational laboratories and test facilities, supporting a large and growing team of engineers and technicians.
We are currently recruiting for two Regulatory Specialists to join a Milton Keynes based company, in a 1-year fixed term contract.
Overview
The successful candidate will support internal customers including: Customer Service team, Sales reps, Research & Development team, and Quality Assurance team by serving as an expert in assigned areas.
As a Regulatory Affairs Professional, you will assume a crucial role in providing leadership and expertise in all regulatory and submission-related aspects of clinical trials.
We are partnered with a leading Pharmaceutical organization who are looking for an experienced Regulatory Consultant to join on a 12-month contract basis.
You will work as a Regulatory EU CTR SME and support several EU CTR submissions.
Regulatory Legal Counsel, 12 month Fixed Term Contract
Our client, based in Redhill, an exceptional financial services organisation who operate globally, are looking for an individual to join the small legal team, to deliver legal services, advice and support to the business to ensure legal risks are appropriate, identified and managed.
You will devlop and adhere to relevant policies and procedures to identify and manage legal risk, along with management of external legal counsel and advice, as directed by Head of Legal.