This grant opportunity includes several important compliance, regulatory, and special considerations that applicants must address:
Regulatory Compliance:
- Clinical Research: If your project involves clinical research within the UK's National Health Service (NHS), public health, or social care, you will need to complete a 'Schedule of Events Cost Attribution Tool' (SoECAT). This tool helps ensure appropriate steps are taken to attribute, calculate, and manage research costs and potentially secure National Institute for Health and Care Research (NIHR) support.
- Animal Research: Any research involving vertebrate animals or other organisms covered by the Animals (Scientific Procedures) Act requires specific documentation and adherence to welfare standards consistent with UK legislation, even for overseas research.
- Human Participation/Tissues: Projects involving human subjects, their personal information, human tissues, or biological samples require detailed justification, identification of relevant approving bodies, and confirmation of approvals in place.
- Genetic/Biological Risk: You must identify and assess any genetic or biological risks associated with your proposed research and outline your mitigation plans.
Data Protection and Privacy:
- Your application must include a data management plan that clearly details how you will comply with MRC's published data management and sharing policies. This plan should cover data quality, sharing, and security, and refer to any institutional and study data policies. If your organization is ISO 27001 compliant, include the registration number.
- Personal data handling will adhere to UK data protection legislation.
Intellectual Property (IP) and Collaboration Agreements:
- Industry Collaboration Framework (ICF): If your project involves collaboration with an industry or company partner (defined as an enterprise marketing goods or services), you will likely need to follow the MRC's Industry Collaboration Framework (ICF). This framework specifies conditions around intellectual property (IP) arrangements (e.g., ownership of 'foreground IP' developed during the project, rights of industry partners to use academic IP, and any restrictions on dissemination of results).
- Formal Agreements: For audit purposes, UKRI requires formal collaboration agreements to be in place with all project partners if an award is made. These agreements must be signed by all parties before the grant starts.
Ethical Standards and Responsible Research and Innovation (RRI):
- You are required to identify and evaluate all relevant ethical or RRI considerations related to your proposed work and explain how you will manage them. This aligns with MRC's guidance on ethics and approvals.
Risk Management and Trusted Research and Innovation (TR&I):
- Project Risks: Your 'Approach' section must comprehensively identify any risks to delivery of the project and detail how they will be managed.
- International Collaboration Risks: If your project involves international collaboration in a 'sensitive research or technology area', you must demonstrate how it complies with UKRI's 'Trusted Research and Innovation' (TR&I) principles. This includes listing countries involved and identifying if the project relates to any of the 17 areas of the UK National Security and Investment (NSI) Act, along with risk mitigation controls.
Special Considerations and Unique Aspects:
- Transition to Independence: This grant's core purpose is supporting individual researchers to establish their independence. Your application must unequivocally demonstrate your commitment to becoming a sole intellectual leader.
- Host Organization Commitment: A strong statement of support from your host research organization is paramount. It should detail how the organization will support your career trajectory, integrate you, provide mentorship, training, and resources (including space and equipment) beyond the grant's end to foster your continued independence.
- Team Science: While you must lead, the grant encourages team science and interdisciplinary research. You can include project co-leads and specialists whose expertise complements your own, but your leadership role must remain clear.
- Diversity and Inclusion: Beyond general EDI commitments, the grant emphasizes embedding diversity into research design (e.g., considering diversity in human study populations and using male and female animals/tissues in research, with justification if not).
- COVID-19 Impact: Reviewers will be advised to consider the unequal impacts that COVID-19 related disruptions may have had on applicants' career development and ability to deliver research.
- Public Partnerships: Encouraged and can include costs for public contributors (e.g., people with lived experience) as 'specialists' in your core team.