CANDIDATES
EMPLOYERS
TOOLBOX
Seltek Consultants Limited,
25a Hockerill Street,
Bishop's Stortford,
Hertfordshire,
CM232DH
UK
Tel: 01279 657716
Email: sales@seltekconsultants.co.uk

|
|
Regulatory (8)

COREC
Central Office for Research Ethics Committees (COREC)

DG III-E-3
EC Directorate General for Industry, Pharmaceuticals and Cosmetics Uni

EEC-MRFG
European Heads of Agencies site - lists all European regulatory agencies and links to their sites

EFGCP
European Forum for Good Clinical Practice

Food and Drug Administration
FDA forms can be downloaded from forms.psc.gov/

ICH
Download those ICH guidelines

MHRA
The MHRA was formed from a merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA) on 1 April 2003.

NICE
National Institute for Clinical Excellence
Back to the link directory index page
If you know of any web sites that you feel should be listed in this directory please email the details to steve@seltekconsultants.co.uk
Websites that reciprocate our link will be listed alphabetically at the top of each category. |
|
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
|