Clinical Research Coordinator
This role is focused on supporting clinical studies, working closely with investigators and study staff to ensure a smooth execution.
Assist with project planning, including budget development and contract negotiation.
Develop relationships with investigators and study staff.
Participate in training to understand the role of a CRA (Clinical Research Associate).
Prepare and distribute project status reports and study event memorandums.
Support maintaining electronic document-tracking systems for all documents associated with clinical study start-up and execution.
Qualifications:
Bachelor's degree in a related field.
Knowledge of ICH GCP regulations.
Experience in research an asset.
Proficiency in basic software applications.
Job Details:
Seniority level: Entry-level.
Employment type: Contract.
Job function: Research and Analyst.
Industry: Healthcare.