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.
My client, a rapidly expanding outsourced company, are seeking to employ a Pharmacovigilance Project Manager whose primary responsibility will be the delivery of Pharmacovigilance Services and will be the main point of liaison within the company for the client and associated third-party vendors.
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.
This leading biotech company located in Cambridge are currently looking for a Regulatory Affairs Senior Manager to join their Oncology team on a 12 month contracting basis.
The purpose of this role will be to plan and manage regulatory submissions for Oncology products e.g. Clinical Trial documentation and Marketing Authorisation applications, with a focus predominantly on the European markets. ...
Drug Safety Specialist (12 Month Contract) – Cambs / Herts / East Anglia
An exciting 12 month contract has come about with my client, a leading Biopharmaceutical company, for a Drug Safety Specialist. This position will act as a Quality Control for the cases entered onto the database. Previous experience of case processing is needed to be able to check the reports for accuracy. Candidates must be eligible to work in the UK. ...
Clinical Project Manager/Clinical Operations Manager/CPM/PM: A great mid-sized CRO is looking to further expand their UK Clinical Operations team with the addition of an experienced Clinical Project Manager or Clinical Operations Manager. This is a really exciting role for a PM looking to further their career with the support of a company with an international presence. They offer an autonomous working environment and it is a great opportunity for a CPM to join a smaller team.
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.
Senior Medical Writer (Contract) –Home-based An exciting opportunity to join a fast paced and dynamic team in one of the leading CROs in the world. The Senior Medical Writer researches, creates and edits all documents relating to clinical trials. You will be the primary contact for medical writing projects, setting timelines, providing leadership and running training to support more junior writing staff. ...
Quality Systems Manager, East Anglia / Cambridge Global Pharmaceutical Company
Quality Systems Manager required for a leading Pharmaceutical manufacturing site. You will be responsible for the implementation of quality improvement programs and will work closely with QA and plant management teams to assure systems are effectively implemented and maintained to ensure compliance with regulatory requirements. This is a permanent role and candidates must be eligible to work in the UK. ...
Production Manager, East Anglia, Global Pharmaceutical Company Production Manager required for a leading Pharmaceutical manufacturing site. You will have overall responsibility for the management of Production, and implementing the Quality policy, procedures and GMP in the department in accordance with Corporate requirements. Permanent role based in East Anglia. ...
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