List of Required Information for Grant Application:
1. Contact Information: Provide contact details for the person responsible for the grant application, including name, address, phone number, and email.
2. Project Title: Provide a clear and concise title for the proposed project.
3. Project Summary: Write a brief summary of the proposed project, highlighting its objectives, significance, and expected outcomes.
4. Project Description: Provide a detailed description of the proposed project, including the research question, methodology, and timeline. Explain how the project will address the impact of social determinants of health (SDOH) on adverse cancer control outcomes.
5. Budget: Prepare a detailed budget for the proposed project, including a breakdown of expenses and justification for each item.
6. Research Center Expertise: Describe the relevant expertise and insights that make your research center well-suited for this grant opportunity. Highlight any previous experience or success in addressing cancer control equity and social determinants of health.
7. Collaboration Plan: Outline a plan for meaningful community collaborations, including how you will engage and involve local communities in the research process. Describe any existing or potential partnerships with community organizations.
8. Data Management: Explain how your research center will contribute to the management and sharing of consortium-wide data. Discuss any data infrastructure, platforms, or systems you have in place or plan to develop.
9. Capacity Building and Training: Describe how your research center will connect with capacity building and training opportunities for researchers, community partners, and other stakeholders. Explain how you will disseminate synthesized research products, findings, and tools.
10. Consortium Collaborative Activities: Outline your plan for stimulating and coordinating collaborative activities within the consortium. Indicate how you will contribute to the overall goals of the ACCERT Consortium.
11. Evaluation Plan: Describe how your research center will evaluate the impact of the consortium. Explain the specific metrics or indicators you will use to measure the success of the project.
12. Clinical Trial (Optional): If applicable, provide details on any clinical trial components of the proposed project. Include information on the study design, participant recruitment, and data collection procedures.
13. Pre-Application Webinar: Indicate your interest in attending the pre-application webinar. Provide your availability and preferred mode of participation (in-person or virtual) if specified.
14. Additional Documents: Include any additional documents or supporting materials that are required for the grant application, as specified in the NOFO.
