Status:
Hours:
Reporting To:
Description
Responsibilities
- Conducting clinical trials in accordance with ICH GCP and TCPS guidelines
- REB submissions, collecting and maintaining regulatory documents.
- Recruiting patients for clinical trials; assessing inclusion/exclusion criteria and determining eligibility with the study investigator.
- Performing all aspects of study visits - informed consent process, all visit activities, collecting data, completing CRFs (electronic and paper), maintaining source documents, and scheduling follow-up appointments.
- Entering and maintaining data in the electronic system
- Processing and ordering supplies for study activities
- Processing and shipping lab specimens to central laboratory
- Communicating with trial sponsors with regards to study documentation, data clarifications, monitoring visits, and audit processes.
Qualifications, Skills, And Knowledge
- Bachelor's degree required; graduate or professional degree an asset
- Proven interpersonal skills, self-directed, and ability to work independently and as part of a team
- Excellent written and verbal communication skills
- GCP, TCSP2, NIH PHRP training, and previous clinical research experience preferred
- Experience with REB and CTO application and amendment documents preferred
- Fully proficient in MS office, and the ability to work with computerized databases
- Data collection and management experience, REDCap an asset
- Sunnybrook experience preferred
Application Instructions:
