Research organisations
Methodological and analytical partnership for universities, institutes and research consortia — without treating QData Intelligence as a CRO by default.
Who this is for
Principal investigators, biostatistics units, clinical research offices and consortia that need study design, statistical collaboration or documentation quality support while retaining scientific and sponsor ownership.
Typical problems
- Study design support before protocols are locked
- Statistical collaboration for complex or multi-site programmes
- Documentation quality that must withstand internal or external review
- Limited in-house capacity without wanting a full CRO takeover
- Need for clear role boundaries with academic governance
How we approach research collaborations
We partner on methods and analysis — scoped engagement, not default outsourcing of sponsorship. Stages follow How we work:
- Discover — scientific aims, constraints, data and governance context
- Frame — advisory vs delivery scope; what remains with the institution
- Build — design input, analysis plans, statistical support, documentation structure
- Harden — reproducibility-minded reporting and handoff for local ownership
- Hand over — institution remains accountable for ethics, sponsorship and publication decisions
What we typically deliver
- Clinical study design and methodology advisory
- Biostatistics collaboration and analysis support as agreed
- Documentation structuring for complex research programmes
- Clear written scope so roles stay unambiguous
Boundaries
- We are not a CRO-of-record unless a specific contract says so
- We do not act as ethics committee or guarantee study/regulator outcomes
- No identifiable patient data via the public website
Relevant expertise
Ready to discuss a programme?
Tell us about your organisation and the type of support you need. Do not send PHI or confidential regulatory packs through the public form.