Coordinate ALS clinical research at the University of Calgary, applying patient management and clinical trial expertise. This is a full-time position in Calgary.
The ALS Clinical Research Coordinator works within the Department of Clinical Neurosciences and Cumming School of Medicine. Reporting to the Director, this position supports investigator-initiated and sponsor-initiated studies. Key work includes participant education, protocol assessments, ethics documentation, and research accounting.
Key Responsibilities:
- Coordinate comprehensive care for patients participating in ALS clinical trials
- Deliver protocol-related assessments and evaluate research outcomes
- Educate patients and families about studies and investigational compounds
- Prepare submissions, amendments, renewals, and safety reports for CHREB
- Track invoices, expenses, payments, and project financial reconciliation
Requirements:
- Minimum MSc education in science or related field
- Strong clinical research methodology experience
- Three years' clinical research experience in industry drug studies preferred
- Strong organizational, communication, leadership, and interpersonal skills
- Vehicle and cell phone required for study communications and travel
Support ALS patients, research protocols, ethics requirements, and project finances as a Clinical Research Coordinator at UCalgary.
ALS Clinical Research Coordinator in Calgary employer: University of Calgary
The University of Calgary is an exceptional employer that fosters a collaborative and dynamic work environment, making it an ideal place for professionals in procurement. With a strong commitment to employee growth, the university offers numerous opportunities for professional development and advancement, alongside a supportive culture that values high-quality service to campus stakeholders. Located in the vibrant city of Calgary, employees benefit from a rich community and access to various resources that enhance both personal and professional life.
