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CSL Confidential Active Jobs Report dated: Saturday, September 11, 2010

Review more information or apply at http://www.cslrecruitment.com/. Search for the CSL 4 digit code in orange using our Quick Job Search. To discuss a role, call our Candidate Hotline: 01932 219 320. Job status changes by the minute on the site and we recommend you apply via the site to ensure status is still 'Open for Applications'.

Clinical Research Associate

CSL Code: 5215

Job Title
Clinical Research Associate
Target Compensation
£30,000 - £45,999
Job Type
Clinical Study Monitoring/Leadership
Location
Greater Manchester
Employment Type
Permanent Job
Employer Type
Pharmaceutical R&D HQ (Global Or EU)
Seniority
Assistant/Associate, Executive/Officer
Duration
 
FTE Hours
Full Time 35 - 40hrs Per Wk
Vacancy Status
Open For Applications
Date Posted
Fri 5th Feb 2010, 09:58am
Are you a CRA based in the North West? If yes then read on...

This is a fantastic opportunity for a CRA/Snr CRA to work with an industry leading pharmaceutical company. The company is internationally recognised as being at the forefront of innovation, technology and market penetration, with it's core values recognizing the importance of customer satisfaction, environmental awareness and the value of its employees. The succesful candidate will have the chance to work alongside top professionals within the industry whilst gaining experience that is universally recognised.

The role is for an office based Clinical Research Associate to support and work alongside the Clinical Project Manager on a number of ongoing studies within the department. This will involve:

Helping mange site communication issues and monitor recruitment.
Assisting with project specific management.
Assuming an ambassadorial role to facilitate communication with sites.
Assists the CTA in maintainingand ensuring the completeness of the study files.

Qualifications:
A minimum of 3-5 years in a pharmaceutical or Biotech company in the position of a CRA.
A life science degree or nursing qualification.
Excellent understanding of the drug development process.
An up to date knowledge of the requirements of clinical trial documentation and the applicable regulatory framework and awareness of ICH-GCP and other regulations in force is essential
Good organizational, planning and prioritisation skills,with relevant experience and qualifications.
Ability to travel locally and internationally.

Please apply or email your CV directly to Michela@cslrecruitment.com

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