Eligibility and requirements
Grants for research will be awarded to projects deemed worthy of support, provided that the basic equipment and research facilities are available in the institution concerned and that it will provide the necessary administrative services. Such awards will be granted for the purchase and maintenance of animals, expendable supplies, minor items of equipment, payment of graduate students, postdoctoral fellows, technical and professional assistants and patient/survivor/caregiver partners, per patient costs for research participants , open access publication costs, research travel and permanent equipment.
These grants do not provide for personal salary support of the Principal Investigator (PI) and/or Co-applicants nor for institutional overhead costs.
An applicant must hold a firm academic position (as a primary appointment) which allows the individual to engage in independent research activities for the duration of the project and includes the ability to supervise trainees and publish research results.
A researcher designated as the Principal Investigator must be based in, or formally affiliated with, an eligible Canadian Host Institution such as a university, research institute or health care agency. Graduate students, postdoctoral fellows, research associates, Adjunct Professors or Status only appointments (except where they hold a firm academic position at another Canadian institution), technical support staff, or investigators based outside of Canada are not eligible to be a Principal Investigator. Both the Principal Investigator and executive authorities of the Host Institution are required to agree to the terms of the Host Institution/Canadian Cancer Society Agreement included as part of the application, thereby acknowledging and agreeing to all the responsibilities and obligations outlined in that Agreement.
The person named as the PI remains the PI on a grant for the duration of the grant unless given express permission by the Canadian Cancer Society.
Applicants who do not yet hold an eligible position
Investigators who have a firm offer of an academic position (as defined above) at an eligible Host Institution and where the appointment is not contingent on the success of a pending application, can submit an application as Principal Investigator provided that the position commences by the start date of the grant. In such cases, a letter from an appropriate authority of the Host Institution must be included, which provides clear details as to the exact nature of the appointment (including title and major responsibilities), as well as the expected start date and duration of the appointment.
A researcher designated as Co-Principal Investigator or Co-applicant is a researcher who may or may not have a formal affiliation with the Host Institution, but will take responsibility for particular administrative and scientific aspects of the research project. These categories can include Adjunct Professors or Status only appointments. These categories may not include graduate students, postdoctoral fellows, research associates, technical support staff, or investigators based outside of Canada. These individuals are not eligible to receive salary support from a grant.
A third category, Additional Authors, formally recognizes other individuals who will make substantial intellectual contributions to the research project or have contributed to the drafting of the application itself, but who are not eligible to be included as Co-Principal Investigators or Co-applicants. Students, postdoctoral fellows, research associates lay contributors and investigators based outside of Canada may be included in this category. Students, post-doctoral fellows and research associates may receive salary support from a grant.
A fourth category, Knowledge Users (or Implementers/Decision-makers, depending on the funding opportunity), recognizes members of a research team who will use the knowledge and/or implement the approaches or interventions generated through the research in order to make informed decisions about health policies, programs and/or practices. Healthcare practitioners, policy makers, educators, decision makers, health care administrators, members of First Nations, Inuit, Métis and Urban Indigenous communities and organizations or racialized communities may be included in this category. CCS staff members participating on grants are to be included in this category. Individuals with lived or living experience of cancer are to be assigned as Patient/Survivor/Caregiver participants. Knowledge Users are not eligible to receive salary support from a grant. In some instances, exceptions may be made, but will be evaluated on case-by-case basis. Please contact CCS to discuss.
Patient/Survivor/Caregiver participants are defined as individuals who have been affected by cancer. This category may include anyone at elevated risk of cancer, who has been diagnosed with cancer, or someone who provides physical and emotional care to someone with cancer, but not in a professional or vocational role. Patients/Survivors/Caregivers are eligible to receive financial remuneration from the grant for their participation (in line with CCS policy)
Any question of eligibility or unusual circumstances not described above will be reviewed and an assessment by CCS will be made.
The following may be required from all participating institutions, depending on the proposed work:
- If this application involves the use of biological materials, a certificate must be submitted from each institutional Biohazards Committee guaranteeing that the project will be conducted under conditions which satisfy the "Laboratory Biosafety Guidelines", published by the Canadian Institutes of Health Research and Health Canada. Please reference their website for current guidelines.
- If this application involves the use of experimental animals, a certificate must be submitted from each institutional Animal Care Committee guaranteeing that all animals will be cared for and studied under conditions meeting the standards stated in the Canadian Council on Animal Care guidelines.
- If this application involves human experimentation, a certificate must be submitted from the appropriate Committee of each institution involved, stating that the protocols and methods have been found acceptable from an ethical point of view in accordance with the "TCPS 2 - Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans " (TCPS 2 has replaced the 1st edition of the TCPS (1998)), published by the Canadian Institutes of Health Research, the Natural Sciences and Engineering Research Council of Canada and the Social Sciences and Humanities Research Council of Canada.
- Human embryonic stem cell research – Any investigator proposing human embryonic stem cell research must contact the Canadian Cancer Society prior to submitting an application. The Government of Canada has passed Bill C-6, An Act respecting assisted human reproduction and related research that regulates, among other things, the use and creation of human embryonic stem cells. The Act may be found on Justice Canada's website. Its provisions dictate the regulations incumbent on applicants, Host Institutions and the funder in the contemplation of carrying out of research covered by the legislation. This will often involve special ethics and other approval mechanisms (beyond approval via the usual local Ethics Review Board).
The Canadian Cancer Society has endorsed and adopted the Guidelines set forward by the Canadian Institutes of Health Research, entitled Human Pluripotent Stem Cell Research: Guidelines for CIHR-Funded Research. In addition, based on the recommendation of the CIHR-led Ad hoc Working Group on Stem Cell Research, a Stem Cell Oversight Committee (SCOC) has been struck. The SCOC will review applications dealing with human embryonic stem cells and other ethically sensitive human stem cell research to ensure that they are in accordance with CIHR's stem cell Guidelines. As with all ethical approvals, for any research grant involving human embryonic stem cells, it is the responsibility of the applicant to ensure that the work proposed has been approved by the SCOC.
If the application involves the use of human samples, please note that the CCS is committed to ensuring that high-quality ethically sourced bio-specimens are used in research it funds, as these yield high, reproducible quality data. If human samples are included in projects submitted to the CCS, applicants are required to provide one of the following at time of funding:
1) Document that all bio-specimens will or have been collected in accordance with recognized standards, such as the Canadian Tissue Repository Network or equivalent (e.g. CLIA). Adherence to these standards and/or certification will be included as part of the peer review. Participation in external quality assurance programs will be considered eligible grant expenses.
2) Provide a brief description of the source, quality and handling procedure of the samples.
Please be advised that no funds will be released to successful applicants until all required certificates are received.
The support of graduate trainees and postdoctoral fellows are encouraged. CCS no longer utilizes a stipend scale for salaries for trainees. Salaries requested should conform to the Host Institution rate based on the experience of the individual required for the project as of the first year of the project. If the person is unnamed, justify the need for a post-doctoral fellow with the number of years of experience required specifying the work to be undertaken.
Taxation will depend on your Host Institution policy regarding trainees.
Grantees may use up to 5% of the grant budget for legitimate scientific and conference travel. Any monies spent on travel must be accounted for in annual accounting statements.
All grant recipients must submit scientific reports throughout the grant and after the grant end date. Principal Investigators will be emailed instructions about completing the report in our online system (EGrAMS). Submission of these reports is mandatory. Failure to submit the required reports will result in the future installments on a grant being withheld.
Annual progress and end of grant reports
Investigators are asked to provide a summary of scientific progress, a list of publications and presentations associated with the grant, details on trainees, and impacts of their research. Investigators will also be asked to list any activities that have helped to promote CCS.
Post grant reports
As impacts of research may occur beyond the termination date, grantees must submit a “Post Grant” report two years after the grant termination date. The report will capture notable outcomes and publications not previously reported to CCS, status of trainees, etc.
For more information on how we evaluate the impact of our research, please see our research impacts section.
In order to highlight research findings to the public, grantees are requested to contact the Canadian Cancer Society Manager, Research Communications with copies of important preprints and to involve the appropriate office in any media interactions that emanate from the funded research activities. The funder acknowledgement (see below) must be included in any grant announcements.
Investigators are expected to publish their results in peer-reviewed scientific journals, and to present their findings at scientific conferences. Grantees must acknowledge the funder in all scientific communications and media releases related to the grant. Proper acknowledgement would be "This research is supported by the Canadian Cancer Society (grant #XXXXXX)". Grants co-funded /funded by a partner/donor will be advised of appropriate language for the acknowledgement.