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Clinical Trials Assistant Jobs

Company

IQVIA

Address Ontario, Canada
Employment type FULL_TIME
Salary
Category Pharmaceutical Manufacturing
Expires 2023-09-15
Posted at 8 months ago
Job Description
Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Essential Functions
  • Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
  • Assist with periodic review of study files for completeness.
  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
  • Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
Qualifications
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Knowledge of applicable protocol requirements as provided in company training.
  • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
  • Written and verbal communication skills including good command of English language.
  • High School Diploma or equivalent
  • Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
  • Effective time management and organizational skills.
  • Equivalent combination of education, training and experience.
  • 3 years administrative support experience.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com