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Details

Clinical Trials Advisor


Reference:BC/HQ00000295 Location: Limerick
Qualification:DegreeExperience:1-2 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Clinical Project Manager, Clinical Research Associate, Clinical Services Coordinator

Clinical Trials Advisor

Responsibilities:

-Analysis of clinical trial protocols and other client source material
-Build up a thorough knowledge of the trial
-Preparation of study materials for development teams;
-Determine what elements are important to the target audience and the
depth of coverage required in the product
-Script product content to meet client requirements and in-house quality
Standards
-Identify leverage from previous trials
-Resolve clinical queries from the development teams
-Storyboard with Graphic Designers as part of graphic development
-Review and sign-off the product(s) prior to delivery to the client
-Act as the primary point of contact with the client on definition of product content and all
related issues
-Liaise with CROs and trial vendors as required
-Present on behalf of the company at investigator meetings
-Apply clinical expertise in providing input to new product development

Applicant Profile:

Minimum of 3 years 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 (Central Labs, IVRS, Data Management)
Fluent in English language (spoken and written) – additional languages would be
considered an advantage
Excellent time management skills and ability to work to project-driven deadlines

If you would like further Information you can contact the recruiter directly:

Brian Christensen | Tel: +353 (0) 1 685 4747