WHAT WE DO

BC Cancer bccancer.bc.ca provides comprehensive cancer control for the people of British Columbia.
Provincial Health Services Authority (PHSA) plans, coordinates and evaluates specialized health services with the BC health authorities to provide equitable and cost-effective health care for people throughout the province. Our values reflect our commitment to excellence and include: Respect people – Be compassionate – Dare to innovate – Cultivate partnerships – Serve with purpose. Learn more about PHSA and our programs: jobs.phsa.ca/programs-and-services
PHSA is committed to employment equity and hires on the basis of merit, encouraging all qualified individuals to apply. We recognize that our ability to provide the best care for our diverse patient populations relies on a rich diversity of skills, knowledge, backgrounds and experiences, and value a safe, inclusive and welcoming environment.

• Perform the data management aspects of clinical trials, in collaboration with other members of the Clinical Trials and Health Care Team, by performing duties such as:a. Organizing and maintaining study files and documentation.b. Preparing reports and regulatory documents as required, distribution to external individuals and/or groups.c. Ensuring that follow-up tests are completed and deficiencies report.d. Organizing and conducting study start-up and termination procedures with outside agencies in accordance with Federal Guidelines adapted by each sponsor.e. Correlating, organizing, calculating trials data for reports, audits, studies, and other client needs according to established criteria.
• Capture clinical trials data, as specified in the protocol and in collaboration as required with the Clinical Trials Team, by performing duties such as:a. Completing study case report forms and other documents within the required timeframes.b. Retrieving or requesting data by identifying selection parameters for retrieval.c. Obtaining information from the patient, chart, family, or other health care professional as required.d. Utilizing coding systems and resources as required to code and input data as pertaining to Clinical Trials.
• Design and develop clinical trial data collection tools, in collaboration with the Clinical Trials Team, by performing duties such as designing forms, tables, and data definitions.