Clinical Research Site Supervisor

Autismservices; Regina; On-site; CAD 47,000 - 56,000; Full time

Job summary

A leading healthcare provider in Regina is seeking a Clinical Research Site Supervisor to oversee and organize operational activities within the Clinical Research department. This permanent full-time role involves coordinating with patients, healthcare professionals, and sponsors while ensuring compliance with regulatory standards and fostering stakeholder relationships.

Qualifications

• Experience in clinical research and regulatory compliance.
• Strong communication skills for stakeholder engagement.
• Experience in organizing and supervising teams.

Responsibilities

• Plan, organize, and supervise operational aspects of the Clinical Research department.
• Coordinate research requirements for patients and ensure compliance with regulatory standards.
• Participate in quality assurance activities and monitor compliance with practice standards.

Skills

Coordination

Compliance Monitoring

Stakeholder Engagement

Quality Assurance

Education

Relevant Degree in Health Sciences or related field

Job description

Pay Band 9 $47.458 to $55.087 (5 step range)

Posted Date: 11-Jun-2025

Location: REGINA

# of Positions: 1

Employment Terms: Full Time

Length of Employment: Permanent

Apply By: 18-Jun-2025

How to Apply: Visit the employer website.

Application Information

Employer Name: SASKATCHEWAN CANCER AGENCY

Closure Date: June 17, 2025 12:00 AM CST

Position #: 205882

Union: Saskatchewan Government and General Employees Union

Bargaining Unit: SGEU - Saskatchewan Cancer Agency

City/Town: Regina

Facility: Allan Blair Cancer Centre

Department: Clinical Research

Type: Permanent Full-time regular

Expected Start Date: June 30, 2025

FTE: 1

Shift Information: Days

Hours of Work: 3 week rotation

Salary or Pay Band: Pay Band 9, $47.458 to $55.087 (5 step range)

Job Description: As a member of the Care Services Division, the Clinical Research Site Supervisor reports to the Director of Clinical Research. The supervisor is responsible for planning, organizing, and supervising operational aspects of the Clinical Research department. They establish and maintain links with stakeholders such as patients, health professionals, sponsors, SHA, University of Saskatchewan, and patient/family advisory groups. They coordinate research requirements for patients, ensure training for SHA staff, support investigator-initiated trials, and ensure compliance with regulatory standards. They also reconcile invoices from sponsors and participate in quality assurance activities, monitoring compliance with practice standards, GCP guidelines, and regulatory bodies.