Clinical Data Coordinator

Project Support

• • Assist in essential DM documentation preparation for various trial stages (i.e. start-up, maintenance and closeout)
  • Assist in basic database and edit check testing activities.
  • Perform data review and query generation.
  • Perform data entry where required.
  • Update database to correct errors.
  • Assist with generating SAS requests and reviewing report outputs
  • Assist with generating Data Transfers and reviewing transfer outputs
  • Assist in the completion of all activities necessary for the finalization and transfer of clinical database and relate project documentation to sponsor.
  • Ensure approved study documentation is maintained and properly stored in the trial master files.

Department Support

• • Contribute to the continuous improvement of Data Management and the wider organization through information sharing, training and education.
  • Promote and be an advocate of Data Management internally and externally.

Qualifications

• • Applicants should have a minimum of a one-to-two-year post-secondary certification in a relevant field of study, or a minimum of one to three years of related work experience with ongoing training. The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results. Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results. Ability to engage in continuous learning and self-development. Ability to continually foster teamwork.