Clinical Research Assistant III

at  OHRI

Facilitate the conduct of clinical research involving human subjects under the general direction of Scientists, Clinical Research Associates, and Research Coordinators, the Clinical Research Assistant III will work on preparing and submitting research applications to the research ethics board, help in preparation of grant proposals and manuscripts patient recruitment, data collection, data entry and/or analytical assistance.

BASIC REQUIREMENTS (EDUCATION/EXPERIENCE):

• Bachelor’s degree or certificate in health sciences or related field (e.g., RN or PT etc.)
• 2 year of previous clinical research experience
• A comprehensive understanding of the clinical research process
• Evidence of training in Tri-Council Policy Statement 2 (TCPS2), the international conference of harmonization Good Clinical Practice Guidelines (ICH-GC), and Health Canada Division 5.
• A working understanding of clinical medicine and its norms and language skills required to critically appraise preclinical and clinical studies.
• Superior organizational and communication skills
• Ability to work independently and as a team member.
• Ability to manage multiple projects at one time.
• Ability to organize, coordinate and prioritize own work.
• Attention to detail to ensure accuracy of data and protocol requirements.
• Must be proficient in basic computer software such as MS Word, Excel, PowerPoint, Outlook, OneDrive, Teams, etc.

PREFERRED QUALIFICATIONS:

• Knowledge of EPIC and TOH processes for arranging diagnostic imaging, investigational therapy, and patient follow-up visits
• Previous research experience, publications
• Experience in clinical Neurosurgery or Neurology Knowledge of statistical analysis
• Experience with ethics board procedures/applications
• Grant writing experience
• Experience with clinical trials and databases
• Experience in a preclinical/clinical research environment

Please refer the Job description for details