An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract.
Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved.
Other responsibilities include
You will develop, contribute and ensure the accurate preparation of high-quality regulatory documents needed to support clinical trials and medical products.
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.
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.
Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract.
This is a great opportunity to work for a pharmaceutical company who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.
Key Responsibilities
A key role in the execution of CMC regulatory strategies working on multiple cross functional projects.
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.
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 and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in UK & Ireland.
Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland.