Clinical Research Officer, Canadian Medical Imaging
2 weeks ago
**Clinical Research Officer, Canadian Medical Imaging Inventory**
**Status: Full-time; Term duration: 1 year**
**Location: Ottawa or Toronto, ON (Hybrid)**
**Closing date: January 26, 2023**
**Salary range: $72,895 - $101,761 per year**
******CADTH is Canada’s drug and health technology agency. We’re a not-for-profit organization headquartered in Ottawa, with a satellite office in Toronto. We’re funded by Canada’s federal, provincial, and territorial governments to provide independent information and advice to the country’s publicly funded health care systems. Health administrators and policy experts rely on CADTH to inform their decisions about the funding and appropriate use of the drugs, devices, and services used to prevent, diagnose, and treat medical conditions.
**Primary Focus**
CADTH created the Canadian Medical Imaging Inventory (CMII) to document current practices and developments in the supply, distribution, technical operations, and general clinical and research use of advanced imaging equipment across Canada. The Clinical Research Officer, CMII position at CADTH is at the centre of the work we produce for the Canadian Medical Imaging Inventory and focuses on advanced imaging modalities and related devices.
As a Clinical Research Officer (CRO) within the CMII program, you will be responsible for supporting survey development and implementation; obtaining and cleaning data from various sources; organizing, analyzing and interpreting data; preparing technical analyses and producing reports; developing and implementing advanced models and algorithms; performing statistical analyses; responding to questions about the data and requests for information; and conducting summaries of the literature and other evidence-based analyses. Our CROs work on a variety of projects in a team-based environment and all CROs receive broad training. We also recognize specialized skill sets and facilitate opportunities for our staff to work to their strengths.
**On any given day, the Clinical Research Officer will**:
- Extract and analyze information from a complex database
- Conduct quantitative and/or qualitative analyses to support the development of reports.
- Perform data quality and quality assurance process and fact checking activities
- Conduct research and analyze and summarize information or data
- Prepare reports that effectively communicate research findings in a format that meets customers’ needs (technical reports, briefing papers, manuscripts)
- Present research findings and methodologies to colleagues, customers, and expert and jurisdictional advisory committees, and periodically present at national or international meetings and conferences
- Collaborate with external content experts, reviewers, stakeholders, and others to ensure the successful execution of assigned projects
**Is this the right role for you?**
**The Clinical Research Officer will likely have**:
- A graduate degree, preferably in a health-related discipline, accompanied by a minimum of one (1) full year of relevant research experience
- Experience conducting data analysis using SAS, R or Power BI
- Strong analytical and critical thinking skills with the ability to extract and analyze information from a complex database
- Knowledge of research theories, principles, practices and methodologies and systematic inquiry, situational analysis, and reflective practice skills
- Excellent written and oral communication skills and demonstrated strength in scientific or technical report writing
- Excellent interpersonal skills and the ability to work effectively with multidisciplinary teams, advisory committees, and external reviewers and experts (including the ability to review and provide feedback on others’ work and to respond constructively to feedback on your own work)
- The ability to work independently, and to prioritize and manage multiple projects to meet competing deadlines
- The drive to learn more and to see a job done well
- The courage and confidence to suggest improvements, present opinions, and articulate conclusion
- Proficiency with Microsoft Word, Excel, and Outlook
**What Will Set You Apart?**
- Training in epidemiology, health technology assessment, or related disciplines
- An understanding of the principles of evidence-based medicine and study designs for health studies
- Training or experience in conducting, reviewing, or critically appraising health-related studies, including observational studies
- Experience with survey design, conducting surveys, semi-structured interviews, or consultation and analysing the information gathered
- An understanding of the Canadian health care system, and knowledge of the decision-making processes for drugs and other health technologies at the federal, provincial, and territorial levels
- Experience in reviewing and critically appraising qualitative research
- Having established networks within the health sector research community
- Fluency in French
**What’s in it for
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