Clinical Research Pro — Oncology Trials & Regulatory Ethics

Winnipeg Regional Health Authority; Winnipeg; On-site; CAD 60,000 - 85,000; Full time

Job summary

CancerCare Manitoba is seeking a Clinical Research Professional (CRP) to play a pivotal role in the Clinical Trials Unit, reporting to the Unit Manager. The CRP will screen and recruit participants, explain non-interventional studies, obtain consent, and ensure protocol adherence while coordinating with sponsors and internal teams.

The role involves preparing and submitting regulatory approvals, managing study data and files, and liaising across departments to keep trials compliant and on track.

Qualifications

• Post-secondary education in a related health care field plus research-related experience; an acceptable combination of education and experience may be considered.
• Demonstrated ability to work effectively both independently and as part of a multidisciplinary team.
• Excellent communication and interpersonal skills; ability to explain complex information to diverse audiences.
• Proficiency with Microsoft Office applications and data handling.

Responsibilities

• Screen and recruit eligible participants for active research studies according to protocol and regulatory requirements.
• Explain study details to participants and obtain informed consent/assent for non-interventional trials.
• Ensure study protocol adherence by extracting, compiling, and submitting patient data; manage study files.
• Prepare, submit, and follow up on committee and board approvals required for conduct of clinical research.
• Coordinate with study sponsors and internal departments to ensure smooth project operation.

Skills

Teamwork

Communication

Microsoft Office

Attention to detail

Problem solving

Education

Post-secondary education in a related health care field

Research-related experience

Job description

CancerCare Manitoba is seeking a Clinical Research Professional (CRP) to play a pivotal role in the Clinical Trials Unit, reporting to the Unit Manager. The CRP will screen and recruit participants, explain non-interventional studies, obtain consent, and ensure protocol adherence while coordinating with sponsors and internal teams.

The role involves preparing and submitting regulatory approvals, managing study data and files, and liaising across departments to keep trials compliant and on track.