- Drug Safety Specialist - West London
Drug Safety Specialist - West London
A rare opportunity has become available for an experience Drug Safety Specialist to join this industry leading company. The successful Drug Safety Specialist will need to have experience in regulatory reporting and a good understanding of case processing.
- Drug Safety Associate – Berkshire/Buckinghamshire
Drug Safety Associates required to join a thriving dynamic company. A position has become available for an experienced Drug Safety Associate to join this world leading CRO on a permanent contract and gain great experience within all sectors of Drug Safety.
- Drug Safety Specialist - Berkshire/Buckinghamshire
Drug Safety Specialist - Berkshire/Buckinghamshire
A rare opportunity has become available for an experience Drug Safety Associate to join this industry leading company. If you are passionate about drug safety and crave career progression then this dynamic company will be the perfect fit.
- Drug Safety Associate - Berkshire/Buckinghamshire
Drug Safety Associate - Berkshire/Buckinghamshire
A Drug Safety Associate is required to join one of my top clients. If you are a hard working Drug Safety Associate that is able to adapt to a fast paced environment and serious about a career within Drug Safety then get in touch. My client is offering the successful candidate a lucrative salary package and career progression.
- Drug Safety Specialist (12 MONTH CONTRACT) – Cambs/ Herts /East
Drug Safety Specialist (12 MONTH CONTRACT) - Cambs/ Herts /East Anglia
A rare opportunity has arisen with a leading Biopharmaceutical company for a Drug Safety Specialist to join on a lucrative 12 month contract. The position will act as Quality Control for cases entered onto the Database. Previous experience of case processing is needed to be able to check the reports for accuracy.
- 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. ...
- Quality Associate
QA Associate required for leading Pharmaceutical manufacturing company. This position isn open to graduates who have a passion for Quality and are looking for their fist role. You will be responsible for QC checking, batch and document review and reports into non-conformances and CAPAs. Candidates must be eligable to work in the UK. ...
- Regulatory Affairs Manager CTA – West London
Regulatory Affairs Manager CTA - West London
My client, a dynamic company which is globally recognised as an extremely reputable company has an urgent opening for a Regulatory Affairs Manager CTA. The successful candidate will join the EU Regulatory Team based in the UK.
- 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. ...
- 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. ...