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Clinical Trial Assistant


  • Global Channel Management, Inc.
  • 10/30/19
  • Madison, NJ
  • 07940
  • $25 / Hourly
  • Full-Time
Clinical Trial Assistant needs 1-2 year relevant experience in pharmaceutical industry or CRO
Clinical Trial Assistant requires:
Experience supporting clinical trials preferred
Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus
Proficiency with Microsoft Word, Microsoft PowerPoint, Microsoft Outlook, and Adobe Acrobat
Strong skills with Microsoft Excel required
Experience using electronic data capture (EDC) systems is a plus
Must possess excellent skill/ability in the following:
Oral and Written Communication
Organizing
Judgment and Problem Solving
People Relationships
Bachelor's degree or higher

Clinical Trial Assistant duties:
Supports the Clinical Trial Management/operational study teams in the execution and delivery of studies
Support study feasibility activities and perform database/web searches for sites as needed. Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.
Organize and maintain project working files and track critical documents. Report discrepancies to the appropriate clinical team member in a timely manner.
Reconcile and transmit all essential documentation to CDIC as per Forest policy.
Track and assist with processing site/vendor payments. Follow up on any issues as required.
Collect and track patient enrollment information and update study management reports as necessary.
Participate in testing of specifications and edit checks for internal (i.e. electronic data capture (EDC) and external (e.g. Interactive Voice/Web Response Systems (IVRS/IWRS), laboratory vendors) systems.


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