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Clinical Trials Assistant

Job Description

May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Primary Duties:
  • The Clinical Trials Assistant (CTA) will support the clinical project team in the following areas
  • Accurately update and maintain clinical systems within project timelines;
  • Prepare, handle, distribute, file, and archive clinical documentation and reports
  • Review of study files periodicallyfor accuracy and completeness
  • Prepare, handle and distribute of Clinical Trial Supplies and maintenance of tracking information
  • Track and manage Case Report Forms (CRFs), queries and clinical data flow.
Requirements:
  • School diploma/certificate or educational equivalent; or equivalent combination of education, training and experience; BS/BA preferred
  • Must possess a general knowledge of applicable clinical research regulatory requirements; including GCP and ICH guidelines
  • Strong Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.

Job Requirements

 

Job Snapshot

Location US-NC-Durham
Employment Type Contractor
Pay Type Hour
Pay Rate $0.00 - $22.00 /Hour
Store Type Clinical & Scientific, Other
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Company Overview

Ascent

The Ascent Services Group (ASG) is a leading national technology consulting and professional services firm that focuses on tactical and strategic consulting. ASG’s fundamental business is providing staffing services to Large Enterprise clients in our core market verticals: Financial Services, Healthcare, and Life Sciences. We focus the majority of our efforts in Staff Augmentation support of Large Enterprise Clients who utilize a Vendor Management System. Learn More

Contact Information

US-NC-Durham
Jessica Latraille
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Snapshot
Ascent
Company:
US-NC-Durham
Location:
Contractor
Employment Type:
Hour
Pay Type:
$0.00 - $22.00 /Hour
Pay Rate:
Clinical & Scientific, Other
Store Type:

Job Description

May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

Primary Duties:
  • The Clinical Trials Assistant (CTA) will support the clinical project team in the following areas
  • Accurately update and maintain clinical systems within project timelines;
  • Prepare, handle, distribute, file, and archive clinical documentation and reports
  • Review of study files periodicallyfor accuracy and completeness
  • Prepare, handle and distribute of Clinical Trial Supplies and maintenance of tracking information
  • Track and manage Case Report Forms (CRFs), queries and clinical data flow.
Requirements:
  • School diploma/certificate or educational equivalent; or equivalent combination of education, training and experience; BS/BA preferred
  • Must possess a general knowledge of applicable clinical research regulatory requirements; including GCP and ICH guidelines
  • Strong Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.

Job Requirements

 
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Clinical Trials Assistant Apply now