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Seltek Consultants Limited,
25a Hockerill Street,
Bishop's Stortford,
Hertfordshire,
CM232DH
UK
Tel: 01279 657716
Email: sales@seltekconsultants.co.uk
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 We handle many vacancies for experienced Drug Safety Scientists. Below you'll find an examples of typical Drug Safety Jobs.
DRUG SAFETY MONITOR |
| Our client, a leading global contract research organisation with offices throughout Europe, the USA, Asia Pacific, South America and South Africa, has an opening for an experienced pharmacovigilance professional to join their medical safety team as a Drug Safety Monitor based in the South of England. In this rôle you will be responsible for tracking and processing adverse events and other drug safety information from clinical trial and post marketing surveillance projects. You will work closely with the clinical development, data management and regulatory departments to ensure that all adverse events are communicated to the applicable regulatory authorites within the UK and overseas. The successful candidate will have a life science degree or relevant qualification and at least one years experience in a drug safety rôle. Experience of reporting SAEs within a European/global environment would be a distinct advantage. You must be a good communicator and confident dealing with industry professionals of all levels. There is an attractive remuneration package on offerto the right candidate including pension, healthcare, life assurance and holday pay. This is an excellent opportunity to gain pharmacovigilance experience within the European environment and is not to be missed! Call us today to discuss this opportunity in the strictest of confidence.
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DRUG SAFETY OFFICER |
A leading pharmaceutical company has an urgent requirement for an experienced Drug Safety Officer to complement their existing safety reporting group based in the South East on a short term contract. You will be responsible for the identification, reporting and follow up of serious adverse events on a worldwide level for a number of products across several therapeutic areas. There is a competitive hourly rate available to the successful candidate plus holiday pay and other negotiable benefits. This is an excellent opportunity to consolidate further your exisiting pharmacovigilance experience within a blue chip pharma environment!
The successful candidate will have a minimum of 1-2 years' experience in a similar rôle within a pharmaceutical company co-ordinating SAE's from both clinical trials and marketed products. |
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DRUG SAFETY ASSOCIATE |
| Gain more experience within pharmacovigilance!This is a great opportunity to join a well respected international contract research organisation entering an exciting period of growth, as a Drug Safety Associate. In this rôle you will project manage the reporting of spontaneous and serious adverse events to European regulatory authorites for investigational and marketed products in phases II-IV of development. There will be an element of database management with this rôle to ensure that all serious adverse events are resolved and updated in accordance with the appropriate guidelines. There will be the opportunity to gain experience within a wide range of therapeutic areas while building upon existing drug safety experience. The successful candidate will have a minimum of one years experience in drug safety combined with previous experience within the pharmaceutical industry in a similar rôle. A BSc in life science or related area is required for this position. Please call us for a confidential discussion about this position and take the first step towards joining an organisation committed to the personal development and training of its employees! |
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LATEST CLINICAL JOBS
A varied and challenging Clinical Research Associate (CRA) role with a leading, specialist oncology research operation in the UK. This organisation is channeling vast amounts of funding into oncology research and in the last two years alone has been involved in the development of various novel cancer treatments.
With increased funding ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in the Netherlands. The role can be office or field based with regular travel to monitoring sites. You will assist in managing large scale clinical trial projects or act as a project manager for small scale projects ensuring on time and on budget performance ... more
This leading CRO is looking to recruit a Project Manager to manage phase IV clinical research projects throughout Europe.
This position has arisen due to expansion, as they have recently won a large number of phase IV proposals.
You will lead the clinical team to ensure on-time, on-budget performance, review and approve regulatory and administrative documents from investigator sites, as well as reviewing CRF’s and SAE reports.
You will also ... more
One of the top ten clinical research organisation (CRO) is expanding, and is keen to recruit a Senior CRA to join their team in Germany...more
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