Job Title: Senior Clinical Research Associate/SCRS/North East
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Vacancy details
Vacancy description:
Job Code:
J014706
Job Title:
Senior Clinical Research Associate/SCRS/North East
Job Category:
Clinical Research
Contract:
Locum/Temporary
Discipline:
CRA
Country:
United Kingdom
Location:
Lancashire, Manchester, South Yorkshire, Staffordshire
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
16 May 2008
This organisation is one of the world’s top ten pharmaceutical companies and is renowned for offering unrivalled career progression across its Clinical, Regulatory, Drug Safety and Medical functions. Opportunities to work for this organisation are rare and are hard fought over.
They are now looking to recruit a Senior Clinical Research Associate. It is a permanent position and field based in the North-East of England.
The main purpose of the Senior CRA role is to identify, select, monitor and close out investigator sites in compliance with SOPs, ICHGCP and the UK Statutory Instrument, so that site performance targets are achieved and that the company’s image with its external customers is enhanced.
Primary Duties:
In this role, you will take responsibility for conducting the SDV and ensuring data is submitted to data management in a timely fashion, you will also manage a number of investigator sites and studies commensurate with your experience, so that studies are run efficiently, and key study objectives are met, ensuring these are run in line with ICHGCP and SOPs and procedures.
You will be responsible for all aspects of site management from site selection to study close-out and will have an understanding of the product, the protocol and the therapy area in sufficient detail to be able to have appropriate discussions with the investigator team. This will include reporting on the progress of all studies at the investigational site after each visit to ensure that all relevant personnel are aware of progress against plan and any issues that have occurred.
Qualifications/Skills/Experience:
The successful candidate is likely to be a life science/nursing graduate or equivalent and have substantial experience as a CRA, having monitored across a variety of therapy areas and trial phases. You will have a thorough knowledge of GCP, and be computer literate (word processing and spreadsheets). Previous experience of electronic data capture is highly beneficial.
As this role involves regular travel a full driving licence is essential.
Keywords: Senior Clinical Research Associate SCRA field based North-East driving licence
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