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CLINICAL TRIAL ADVISOR
Company:CPL |
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Job Reference Number |
14573837 |
Client ID: |
RI/JO-1203-244134 |
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Posted On: |
Feb 28 2012 |
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Location: |
MUNSTER COUNTIES, LIMERICK |
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Job Type: |
Contract |
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Salary: |
NEG |
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Our client a market leader in clinical quality management solutions now have a vacancy for a Clinical Trials Advisor. This is a maternity contract vacancy- duration approx 6-9 months.
Responsibilities:
-Conduct internal review of clinical trial protocols to support both Business Development and Finance.
- Determine protocol specific challenges and identify solutions.
Research the Company database to identify leverage/experience from previous trials
-Advise Finance on intricacy of the study and anticipated production time
-When required attend Client External Kick Off meetings with Project Manager
-Provide Company scripts for Protocol Overview and VBVG to production team in advance of initiation of product production. -Provide production team with study handover presentation
-Prepare the specification for study calculators when required
-Provide Technical review of scripts prepared by other members of the CTA team
-Review and where required apply internal and client edits
-Support production team when required with Protocol Amendments, Graphic Design story boarding and general guidance
-Conduct regular Internal Audit and On Screen Reviews of portals.
-Attend CTPG meetings on a monthly basis
-Represent the Company at Investigator and Clinical Trial Associate Meetings. Report to Head of Clinical Trial Planning Group feedback from study teams, CRA’s and Investigational site Staff
-Attend Client Alliance meetings to ensure the continued improvement of the Company product and client experience
-Ensure all CTPG responsibilities are maintained including but not limited to Protocol Security and Internal Company database
-By means of internal support and individual learning ensure you maintain a high personal level of knowledge concerning current regulation and changes in within the clinical Research industry
Requirements:
-Previous hands-on experience in study delivery or study management
-Excellent knowledge of ICH GCP and other key trial regulations
-Good knowledge of clinical trial services
-Fluent in English language (spoken and written)
-Excellent time management skills and ability to work to project-driven deadlines
For further information please call Linda at 01 2784671 or email your CV in the strictest confidence to [email protected] . Log on to www.thornshaw.com for more jobs.
Keywords:Clinical Trial Advisor, Clinical Trial Assistant, CTA
