Research Assistant

• Support Research Coordinator to oversee the operation and management of research projects.
• Adhere to Good Clinical Practice and incorporate GCP requirements in all stages of research projects from start up to close up.
• Adhere to regulatory and local requirements (i.e. annual safety reports, periodic safety reports).
• Adhere to timelines and milestones.
• Assist with the recruitment and follow up of study participants.
• Compile, review, and file essential documents.
• Collect and transfer study data to the study sponsor using Electronic Data Capture systems such as REDCap.
• Respond to data-related questions and query from internal and external partners.
• Prepare for meetings and teleconferences.
• Help with submission and implementation of Research Ethics Board applicants and amendments.
• Help with publications and other study related documentations.
• Perform activities related to major protocol deviations.
• Creation of data collection forms.
• Regular communication with clinical research team, hospital staff, lead study sites and external parties.

Bachelor's degree in a relevant field of study.
Requires 2 years of relevant experience.

Assets:

• Clinical Trial experience.
• Experience with Canva and other communication and design tools.
• Clinical Trial experience.
• GCP, TCPS2 training.