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Fforde Management
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Senior Clinical Research Associate - Cambridgeshire



Business Type: Clinical Research Organisation
Job Type: Clinical Research, Clinical Research Associate (CRA), Clinical Study- Trials, Senior Clinical Research Associate (SCRA)
Job Level: Not Specified
Position: Full Time
Salary: Competitive
Location: UK - East Anglia
Reference: 17744/002
Closing Date: 11/09/12
Background:

Our Client is an expert Regulatory, Clinical Research and Quality Services consultancy to the healthcare industry worldwide, who focus is on the planning and execution of product development programmes, including a full range of regulatory support services and the management and monitoring of early phase clinical trials. They are currently seeking a Clinical Research Associate for their Cambridgeshire office.

JOB ROLE:
The Senior Clinical Research Associate will be responsible for monitoring clinical trial sites to ensure compliance with the protocol, with GCP and with other appropriate regulations and guidelines The Senior CRA will be the primary contract-point for Investigational site staff and may operate as the lead CRA for multi-centre studies.

PRINCIPAL RESPONSIBILITIES include:
Identification of clinical investigators
Management of the Trial Master file for clinical studies as per GCP
Management of the creation of Investigator site files
Management of the collation of documents for Ethics Committee and study documents at the close of project
Organising and planning of study related meetings
Management of the reporting of adverse events as appropriate
Monitoring of clinical study sites as appropriate, including pre-study, initiation, monitoring and close-down meetings with clinical study investigators

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Degree in Life Sciences
Experience of GCP monitoring in the UK
Exposure to Phase I, II & III would be desirable
Demonstrated ability to work as Lead CRA
Previous mentoring experience would be advantageous
Good understanding of drug development and the clinical trial process

PERSOAL SKILLS & ATTRIBUTES:
Strong communication & interpersonal skills
Good IT skills
Clean driving licence
Availability to travel both domestic and internationally

Fforde is acting as a recruitment agency/business.

KEY WORDS: Clinical Research Associate, CRA, Clinical Trials, Clinical Research, Clinical Studies, Clinical Study, Pharmaceutical, Regulatory, Quality, QC, QA, Drug Safety, Drug Development, Clinical Trial, Cambridgeshire, UK



Posted: 14/08/2012 | NPJ Ref: 85048
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