- Regulatory Manager / Team Leader (Clinical)
• Permanent position
• Innovative pharmaceutical company
• Extensive working knowledge of clinical trial submissions in Europe required
• Development and management of the Regulatory clinical team in Cambridge
- Senior Project Manager/Regulatory Manager: Cambridge
A fantastic opportunity has become available, working for an established health care service provider, dealing with a range of regulatory affairs responsibilities on European and Global level, this company invest heavily to attract and retain high quality staff; this organisation has a very credible reputation for being one of the best employees in its arena. My client invests heavily in talented teams as this is central to their ambitious expansion plans.
- Regulatory Affairs Manager CMC
Manager, Regulatory Affairs CMC – Emerging Markets
My client, a leading Biotech company, with a global presence and highly reputable market presence, is looking for a Manager within their Regulatory Team. This company is rapidly growing year on year and producing products that are changing the world. With more and more MA applications happening each year, their expansion is set to continue exponentially. ...
- Associate Manager
Associate Manager Regulatory Operations (6 month Contract)
A great position has arisen for someone who has experience working within Regulatory Affairs operations or Document control to join one of the leading biotech companies in the world. This role would be ideal for someone who has excellent experience within Regulatory Operations and publishing. You can be part of a team that is literally changing the world and helping millions of people live healthier lives. ...
- Senior Manager/Associate Director - General Medicine Therapeutic Lead - Regulatory Affairs
PPD is seeking a Sr. Manager/Associate Director to join their growing Global Regulatory Affairs (GRA) Department in Cambridge.
In this role, you will provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization.
- Clinical Compliance Manager
An excellent opportunity has arisen for a Clinical Compliance Manager to for an emerging biopharmaceutical company with an excellent pipeline of treatments for oncology in development. The company has an excellent working environment in Cambridge, UK and boast a number of exciting projects to work on. ...
- Regulatory Team Lead (Clinical Manager) UK
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- Associate Director Regulatory Affairs
Associate Director, Regulatory Affairs - Cambridgeshire
A lot of regulatory professionals will be lucky if they get within touching distance of a MAA in a 4/5 year period. My client is expecting to push 1 or 2 out a year. Be part of something big and help it become even bigger!
My client, a leading Biotech company with global coverage and highly reputable market presence, is looking for a Manager within their Pharmacovigilance team. ...
- Clinical Project Manager (Biotech) - Product Development
An excellent opportunity has arisen to work in one of the most exciting areas of modern medicine within this innovative pharmaceutical company.
- Home Based Clinical Project Manager - (Epilepsy)- Biotech
I am urgently seeking an experienced clinical project manager for a permanent headcount position with a small biotechnology company based in Cambridge. The company is licensed by the UK Home Office to work with a range of controlled drugs for medical research purposes. These are very exciting times for my Client and the next few years look set to be the best yet. It would be a great time to join the company right now.