Clinical Research Coordinator III (GI) (Toronto)

Responsibilities

• Recruitment of study participants (identify and screen potential subjects, obtain informed consent).
• Coordinate patient visit schedules as per study protocol.
• Execute all aspects of study visit, including assessment of adverse events, monitoring safety, medication, questionnaires, sample collection, processing and shipment of samples according to clinical protocol.
• Provide clinical care for patients participating in clinical trials and implement and coordinate all aspects of data collection and source documentation within required timeframes, as per UHN policy and ICH/GCP guidelines.
• Other study related activities, as needed.

Qualifications

• Bachelor's degree or recognized equivalent and current certificate of competence (license/registration) from a college legislated under the Regulated Health Professional Act.
• Recognized certification in clinical research (ACRP or SOCRA) obta...