Clinical Research Site Supervisor

As a member of the Care Services Division, the Clinical Research Site Supervisor is under the supervision and direction of the Director of Clinical Research. Clinical Research Site Supervisor is responsible for the daily planning, organizing and supervising assigned operational aspects of the Clinical Research department.

The Clinical Research Site Supervisor works to establish and maintain essential linkages between many diverse stakeholders such as patients, health professionals, sponsors/granting agencies, Saskatchewan Health Authority (SHA), University of Saskatchewan and patient/family advisory group(s). The Site Supervisor ensures coordination of research requirements for those patients admitted to the SHA for treatment, ensures training requirements are met and provided to the SHA staff. Coordination and support of investigator-initiated trials, clinical research projects and sponsored clinical trials while ensuring adherence to regulatory requirements. Reconciles invoices/payments from sponsor/granting agencies.

The Clinical Research Site Supervisor is actively involved in supporting quality assurance and quality improvement activities in the department, which would include; monitoring compliance with nursing and Clinical Research Associate (CRA) practice standards in delivery of patient care, compliance with Good Clinical Practice (GCP) Guidelines, Regulatory bodies and the Clinical Research standard operating procedures. Clinical Research Site Supervisor ensures the work environment enables and supports excellence in nursing and CRA practice and promotes high quality of work life and safety for Clinical Research department staff.

QUALIFICATIONS

Education

• Bachelor Degree in Nursing
• Certification for Basic Life Saver (BLS)-C

Experience

• Five (5) years previous experience working in Oncology Nursing of which three (3) years...

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