Clinical Research Assistant III

at  OHRI

We are seeking a dynamic individual to join the ReThinking Clinical Trials team at the Ottawa Hospital Research Institute located at the Ottawa Hospital Cancer Centre. Facilitate the conduct of clinical research involving human subjects under the general direction of Dr. Mark Clemons, Dr. Marie-France Savard and the REaCT Clinical Research Program Manager. The CRA III is responsible for patient recruitment and follow up, data collection, oversight meetings, and analytical assistance for REaCT clinical trials. Duties would also include assisting in new protocol and case report form development, day to day communication with other participating sites for logistical questions and data collection, completion of regulatory documents, maintenance of all study files and preparation for internal monitoring and audit reviews. This position involves regular contact with both patients and physicians. All REaCT staff also participate in the performance of systematic reviews and literature searches for the REaCT program.

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
• 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.
• 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:

• SOCRA or other certification
• Knowledge of medical oncology
• Knowledge of both official languages

Please refer the Job description for details