Clinical Study Associate (Ottawa, ON)
Allphase Clinical Research Inc. - Ottawa, ON

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  • Prepare, distribute, collect and review all study documentation from sites for accuracy and completeness
  • Liaise with sites to update and correct information in a timely fashion
  • Prepare any study progress reports and attend study team meetings as required by the client
  • Create and maintain any study specific tracking databases as required by the client
  • Ensure client and investigator documentation obligations are being met and are in compliance with applicable regulatory requirements, client SOPs and ICH guidelines
  • Assist the Clinical Study Manager in any functions as required
  • Assist with management and resolution of investigative site queries and requests
  • Work collaboratively with members of the study team to problem solve and promote progress
  • Prepare site payments and track activities
  • Fulfill any other duties as required


  • Undergraduate Degree in Life Sciences
  • At least 2 years of Clinical trials support or pharmaceutical industry experience preferred
  • Proficiency using computerized information systems, Microsoft Office Applications, and electronic spreadsheets required
  • Self-motivated and proactive
  • Good team player with initiative to learn and handle multiple assignments independently
  • Ability to act as a liaison between other functional team members and investigative sites to meet project goals
  • Ability to prioritize and manage multiple projects concurrently
  • Excellent organizational skills and attention to detail

Only suitable candidates will be contacted.

About this company
Allphase Clinical Research is a progressive Contract Research Organization (CRO) dedicated to providing quality and service excellence to...