Clinical Studies Operations Specialist

5 Months ago • 1 Years +

Job Summary

Job Description

The Clinical Studies Operations Specialist will support the conduct of clinical studies according to clinical project timelines. This role acts as a liaison between Clinical Study sites and other internal departments, maintaining clinical study-related documentation. Responsibilities include assisting in study agreement preparation, preparing budget templates, managing clinical site processes, assisting with supply purchasing, preparing documentation for ethics submissions, reporting study-related information to authorities, monitoring and reporting progress, and managing the site administrative support process. The specialist will also prepare on-site documentation, handle study paperwork, and structure the electronic clinical trial master file. This role requires an Associate's Degree and at least one year of clinical trial experience.
Must have:
  • Assist in study agreement preparation.
  • Prepare templates for budget estimates.
  • Manage clinical site referencing and invoicing.
  • Assist with supply purchasing.
  • Prepare documentation for ethics submissions.
  • Report study-related information to authorities.
  • Monitor and report activity progress.
  • Handle study paperwork.

Job Details

Support the conduct of clinical studies related as per clinical project timelines. Act as a liaison person between Clinical Study sites and other internal departments.  Maintain the clinical study related documentation ahead, during and after the completion of the clinical study; work collaboratively with the Clinical Study Scientist and Clinical Research Associate, in conjunction with the clinical sites.

This role is based in Salt Lake City and is not a remote position.

 Job Responsibilities: 

  • Assist in study agreement preparation with legal and other functions along with the concerned authorities at the clinical study sites.
  • Prepare templates for budget estimates and facilitates communication between internal and external partners during contract and budget phases of the clinical study project.
  • Manage the clinical sites referencing, purchase orders, invoicing processes, regular accruals.
  • Assist with supply purchasing and support clinical research associate with supply management
  • Prepare the documentation package for the purpose of the submission to Independent Ethic Committee or Independent Review Board, as per respective expectations
  • Report any clinical study related relevant information to competent authorities (EUDAMED, Sunshine act...)
  • Monitor and report the progress of the above activities to the Clinical Scientist or Clinical Research Associate
  • Own the above site administrative support process
  • Prepare the on-site documentation as per Good Clinical Practices (Investigator Study File - ISF)
  • Handle any study paperwork or electronic documentation generated during the progress of the clinical study
  • Structure, prepare and regularly feed the electronic clinical trial master file, including all the study documentation and main project deliverables.
  • Own the above clinical trial related documentation process

Position Requirements:

·       Associate Degree required

·        1+ years of clinical trial experience 

·       Skills in administrative tools (Office 365 , Teams, Outlook, …), WebApp

·       Team spirit and collaborative work among peers and with department members

·       Excellent sense of customer service

·       Good sense of adaptation, great organizational, ability to prioritize, rigor, methodical approach

 

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