Hematology Clinical Research Coordinator

University of British Columbia; Vancouver; On-site; CAD 66,000 - 78,000; Full time

Job summary

The University of British Columbia in Vancouver, BC, is seeking a Junior Research Coordinator for the Hematology Research Program. The role involves coordinating studies, liaising with clinicians and regulatory bodies to ensure approvals and compliance, and supporting investigators and study teams.

The position requires strong organizational and interpersonal skills, experience in clinical research, and the ability to manage multiple tasks in a fast-paced environment.

Qualifications

• Completion of a university degree in a relevant discipline or technical program.
• Minimum four years of related experience or equivalent education/experience.
• Willingness to respect diverse perspectives, including perspectives in conflict with one’s own.
• Clinical trials experience or background in hematology/oncology is an asset.

Responsibilities

• Conducts multiple studies from startup to closure under supervision of PIs and program leadership.
• Ensures all study activities comply with ICH, GCP, Tri-Council guidelines and SOPs.
• Assists with protocol development, grant applications and regulatory submissions.
• Maintains trial documents, source documentation, CRFs and drug accountability logs.
• Identifies, recruits and educates study participants and informs patients about protocol requirements.
• Coordinates with radiology, laboratory, pharmacy, health records and nursing units as required.
• Provides updates to PIs and Research Managers on study progress and issues.

Skills

Organizational skills

Interpersonal skills

Communication skills

Multitasking

Education

University degree

Graduate degree (optional)

Tools

Microsoft Office

Job description

The University of British Columbia in Vancouver, BC, is seeking a Junior Research Coordinator for the Hematology Research Program. The role involves coordinating studies, liaising with clinicians and regulatory bodies to ensure approvals and compliance, and supporting investigators and study teams.

The position requires strong organizational and interpersonal skills, experience in clinical research, and the ability to manage multiple tasks in a fast-paced environment.