- Senior Pharmacovigilance Officer- Edinburgh
Chiltern is a leading International Clinical Research Organisation with offices across the World. Established in London in 1982, Chiltern International has accumulated extensive experience running clinical trials from Phase I to Phase IV across a broad therapeutic range. Chiltern provides an extensive range of services for both the international and national management of studies.
- Drug Safety Specialist - West London
Drug Safety Specialist - West LondonA 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/BuckinghamshireA 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/BuckinghamshireA 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.
- Senior Regulatory Associate (MA's)
Senior Regulatory Associate (12 month Contract)– BerskhireAn exciting opportunity for an experienced Regulatory professional with at least a couple of years’ experience to step into a fast paced and dynamic Pharmaceutical company. ...
- Senior Regulatory Associate
Senior Regulatory Associate (12 month Contract)– BerskhireAn exciting opportunity for an experienced Regulatory professional with at least a couple of years’ experience to step into a fast paced and dynamic Pharmaceutical company. Join a strong development team focusing on Clinical Trial Applications and submitting them to the relative authoritative and ethical committees. ...
- Regulatory Manager
Regulatory Affairs Manager – CMC – Cambridgeshire / West London Great opportunity for an experienced CMC manager to step into the dynamic world of Biotech. This fast paced and cutting edge company is looking for someone to join them for a 6 month contract and help to lead the CMC department. ...
- Regulatory Executive
Senior Associate, Regulatory Affairs (Emerging Markets) – Bucks/BerksMy client, a global Pharmaceutical company, has a high value position to join their global Regulatory team as a Senior Associate. You will be responsible for new MAA submissions and marketed product maintenance for the Europe, Middle East and Africa region. ...
- Regulatory Affairs Manager
Regulatory Affairs Manager – 12 month contract – West London/MiddlesexAn exciting opportunity has come up for a Regulatory Affairs Manager to be based in the West London/Middlesex area. Responsible for supporting regulatory aspects of a product’s development, primarily in relation to CMC. ...