- Identify eligible participants for various studies.
- Recruitment of study subjects including informed consent process, randomization and implementation of study protocol procedures.
- Maintain screening logs/records.
- Completion of Case Report Forms (CRF’s).
- Collection and transmission of source documents.
- Review of Quality Control Reports and resolution of queries.
- Schedule follow up with study participants as per study protocol.
- Manage drug supply for study participants.
- Arrange consultations with MD’s as necessary.
- Complete local Ethics Committee applications, renewals and study closeout applications.
- Maintenance of study binders and logs.
- SAE management and reporting.
- GCP training renewal.
- Host monitoring visits.
- Education of front line health care staff re:



study protocol and procedures.
- Attend site initiations, investigator meeting, etc.
- Attend weekly study team meetings.
- Undergraduate degree in Health related or Business preferred
- Minimum 2 years of Research/ Clinical Trials experience and data management.
- Demonstrated above average computer skills.
- Knowledge of Epic EMR for patient information.
- Demonstrated above average organizational skills.
- Demonstrated robust initiative and drive and the ability to be self-directed.
- Demonstrated interpersonal, communication and teamwork skills.

📌 Research Assistant (Canada)
🏢 Hamilton Health Sciences
📍 Canada