CCTG is hiring right now for several positions including; Clinical Trial Assistants, Study Coordinators and a Clinical Research Associate. The positions are open at the CCTG Central Operations and Statistics Office located at Queen’s University in Kingston, Ontario. More information about these opportunities can be found on the CCTG Careers Page.
Clinical Trial Assistants
Overview – The Clinical Trial Assistant understands ethical trial conduct and adheres to Group Standard Operating Procedures and Work Instructions. Promotes site adherence to standards in trial conduct. Responsibilities include administrative functions that support trial development, activation, and ongoing conduct, liaising with participating cancer treatment institutions, evaluation of incoming information for accuracy and completeness and other projects as assigned. A full job description and how to apply can be found here.
Overview – The Cancer Research Study Coordinator works within a team based structure to coordinate and oversee national, international and cooperative oncology group, multi-centre, multi-modality clinical trials in cancer therapy, prevention and supportive care. Design, develop clinical trials protocols and data collection modules. Establish and maintain a coherent database. Work collaboratively with participating centres (cancer treatment centres) and trial committees (including investigators, clinical research associates, pharmacists), industry partners and others in an evolving international clinical trials environment. A full job description and how to apply can be found here.
Clinical Research Associate
Overview – Reporting to the Manager, Office of Clinical Trials Management, the Clinical Research Associate will work within a team-based structure to support the conduct of national, international and cooperative oncology group, multi-centre, multi-modality clinical trials in cancer therapy, prevention and supportive care. Responsibilities include: critical evaluation of incoming information, including medical data, for accuracy, relevance and prioritization; assisting in the development of clinical trials protocols, case report forms and other trial related materials; communicating with participating centre staff (cancer treatment centres) to promote and understanding of the trial, and accurate data collection in accordance with ICH-GCP and other relevant guidelines. A full job description and how to apply can be found here.