An overview of our requirements is outlined below. For more information and Proposal submission instructions, refer to the RFSO main document.
Category 1: Science and Methods - Methodologist
Health care decision makers rely on reports and other outputs from CDA-AMC to inform their decisions about the funding and appropriate use of the drugs, devices, and health services. Methodologists contribute to the scientific credibility, methodologic rigour and quality of CDA-AMC's reports. Periodically, CDA-AMC needs contractors to supplement our resources to ensure timelines are met for reports.
We are looking to build a roster of Methodologists who will collaborate with our internal project team by applying appropriate methodologies and producing (a section of) the report as per appropriate forms and templates, within the timeframe outlined for the individual project.
Category 2: Analyses and Reports – Clinical Reviewer
CDA-AMC, at the request of federal, provincial, or territorial decision-makers conducts evidence-based analyses on various health technologies including drugs, medical devices, diagnostic tests, clinical interventions, and models and programs of care. CDA-AMC analyses and reports are used to inform planning and decisions on health system preparedness for or appropriate use of (e.g., funding, adoption, disinvestment, replacement) health technologies. Analyses and reports are customized to address specific requests and methods may include systematic or rapid review, survey, consultation, and/or environmental scanning, as appropriate.
We are looking to build a roster of contributors to CDA-AMC analyses and reports. With the support and guidance of CDA-AMC staff, contributors will lead the development of and execute project plans including data collection, data analysis and report writing using CDA-AMC templates and to CDA-AMC standards.
Category 3: Pharmaceutical Reviewer
To ensure CDA-AMC continues to deliver on targeted timelines, we are looking to build a roster of contributors to CDA-AMC analyses and pharmaceutical reimbursement review reports. With the support and guidance of CDA-AMC staff, contributors will lead the development of and execute project plans including data analysis and report writing using CDA-AMC templates and to CDA-AMC standards.
The role of the contractor is to provide the deliverables of a pharmaceutical reviewer, through authorship of the clinical review report and draft recommendation reports. This role requires coordination with the CDA-AMC team, reporting to the assigned Pharmaceutical Reviews Manager (the project owner), and delivering on time according to the schedule.
Category 4: Health Economist
CDA-AMC conducts analyses and prepares reports which may include critical appraisal of economic models/evaluations, or the development or adaptation of economic models. We are looking to build a roster of contributors to support this work. With the support and guidance of CDA-AMC staff, contributors will lead the development of and execute project plans.
This may include: model development, data collection, data analysis; appraisal and reanalyses of economic models; model validation; communicating concepts and results with experts and committees; and report writing using CDA-AMC templates and to CDA-AMC standards.
