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CSL Confidential Active Jobs Report dated: Tuesday, September 07, 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 Trial Associate

CSL Code: 5272

Job Title
Clinical Trial Associate
Target Compensation
Day Rate/Negotiable
Job Type
Clinical Study Administration
Location
Berkshire/Buckinghamshire, Surrey, Hampshire/iow
Employment Type
Temporary Contract
Employer Type
Pharmacuetical Affiliate/Marketing Company, Pharmaceutical R&D HQ (Global Or EU)
Seniority
Assistant/Associate
Duration
6 - 12mths
FTE Hours
Full Time 35 - 40hrs Per Wk
Vacancy Status
Open For Applications
Date Posted
Mon 8th Mar 2010, 03:57pm
Clinical Trial Associate required for initial 12 month contract role in Hampshire.

Our Global Pharma client is looking for a CTA/CPA with at least 12 months clinical research experience working as a clinical trial administrator within a pharma, biotech or CRO.

Main Duties:
Provide efficient clinical trials administrative support across Phase II - IV
Assist with accurate Clinical Trials Management System data entry and reporting
Assist with clinical document generation, review and revisions.
Attend study team meetings, responsible for production of internal meeting Agendas and Minutes in accordance with department best practices, under the supervision of the Study Manager
Creation and maintenance of tracking systems for deliverables not tracked in CTMS
Assist with clinical compliance to SOPs, procedures and regulatory requirements by actively requesting and accurately completing required forms and documents.
May accompany Study Manager on site visits and/or CRO meetings as^necessary (excluding review of study files).
Assist in co-ordinating effective communication between functions and with external vendors and investigational sites.
Prepare electronic documents to meet company standards, as required for regulatory^submissions and Clinical Study Report publishing.

Minimum Requirements:
Previous experience within a CTA role
Ideally a life sciences degree or equivalent (Not Mandatory)

Unfortunately we are unable to assist if you do not have the work experience stated above, and we will require candidates who can legally work and reside in the UK.

Please apply online or contact Michela on 01932 219 320 or email Michela@cslrecruitment.com

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