| Job Code: |
| J4DD/1107/PVG/SCO/AB |
| Job Title: |
| Drug Safety Specialist- Central Scotland |
| Job Category: |
|
Regulatory And Drug Safety |
| Contract: |
|
Permanent |
| Discipline: |
|
QA, Drug Safety, Pharmacovigilance, Regulatory Affairs, Director, Drug Safety Physician |
| Country: |
|
United Kingdom |
| Location: |
|
Avon, Bedfordshire, Berkshire, Buckinghamshire, Cambridgeshire, Cheshire, Cleveland, Cornwall, Cumbria, Derbyshire, Devon, Dorset, Durham, East Sussex, Essex, Gloucestershire, Hampshire, Herefordshire, Hertfordshire, Humberside, Isle Of Wight, Kent, Lancashire, Leicestershire, Lincolnshire, London - Central, Manchester, Merseyside, Norfolk, Northamptonshire, Northumberland, North Yorkshire, Nottinghamshire, Oxfordshire, Rutland, Shropshire, Somerset, South Yorkshire, Staffordshire, Suffolk, Surrey, Tyne And Wear, Warwickshire, West Midlands, West Sussex, West Yorkshire, Wiltshire, Worcestershire, Aberdeenshire, Angus, Argyll, Ayrshire, Banffshire, Berwickshire, Arran And Bute, Caithness, Clackmannanshire, Dumfriesshire, Dunbartonshire, East Lothian, Fife, Forfarshire, Inverness-Shire, Kincardineshire, Kinross-Shire, Kirkcudbrightshire, Lanarkshire, Midlothian, Moray, Nairnshire, Orkney, Peeblesshire, Perthshire, Renfrewshire, Ross & Cro |
| Min experience: |
|
1 years |
| Annual salary: |
|
Negotiable (20000 - 33000 £) |
| Apply by: |
| 30 Jul 2008 |
|
Are you looking to develop your career with a leading Clinical Research Organisation (CRO) and move your career to the next level? If so, then read on.
We are currently working on behalf of a leading CRO based in Glasgow which is currently undergoing unprecedented growth and is therefore seeking to recruit a number of experienced Drug Safety Specialists to join its established team. Successful candidates will become key members of a expanding Pharmacovigilance (PVG/ Drug Safety) team providing effective PVG/ Drug Safety services. You will liaise with study sites and sponsors on safety related issues, interface with other departments, deliver related activities and be responsible for managing the production of various reports and documentation.
The successful candidates will have a minimum of 12 months prior experience either working for a CRO or Pharmaceutical company in a Drug Safety / PVG role or have worked as a Research Nurse within Clinical trials or similar research environment. Excellent interpersonal, communication and team working skills are a prerequisite.
Interested? Call Andy on 0131 473 2343 or email a copy of your CV to andy@squarepegs.biz
Keywords: Pharmacovigilance Specialist, Drug Safety Specialist, Pharmacovigilance, clinical research, Serious Adverse Effects, SAE, Safety reports, Clinical trials, Scotland, Central Scotland, Edinburgh, Glasgow. |
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