Navigating the complex landscape of research governance can bottleneck any project. I can turn your finalised research idea into an operationally defined study and produce the high-quality documentation required to secure funding, sponsorship, and NHS delivery.
This service is fully scalable and can be tailored to your project’s stage of development and your team’s expertise.
I manage the essential structural and regulatory components needed to move your study from concept to clinical practice. Here’s how I help:
Documentation & material design
This is where I create protocol-compliant materials and the data collection tools. Public and patient involvement and engagement are embedded into developing the study materials from the start.
Governance, ethics and IRAS submissions
I prepare robust ethics applications, governance documentation, and transparent financial structures that align with NHS costing models. I also provide preparation and submission support through IRAS to efficiently secure HRA and NHS REC approvals.
Site mapping and activation planning
I evaluate target populations, clinical settings, and recruitment strategies to ensure your project’s overall viability. This process identifies potential barriers and helps to prevent disruptions to your project timeline.
Securing regulatory approval and setting up your study is just the beginning. While your operational team manages data collection, ultimate success depends on understanding how and why those outcomes were achieved. I conduct independent, rigorous qualitative process evaluations, looking beyond raw numbers to capture the real-world experiences of patients and staff to help you influence policy, secure market access, or scale.