Embedded communication, dissemination, & ethics support for EU and Nationally funded research projects

Reducing proposal risk and ensuring long-term compliance in publicly funded research.

    • Dissemination, ethics communication, and participant-facing materials are usually added late

    • Reviewers increasingly scrutinise:

      • Public engagement

      • Ethics & participant comprehension

      • AI / digital communication governance

  • Single point of contact in your project infrastructure for all patient facing comms.

    • Dissemination & impact compliance

    • Participant-facing communication (trials, cohorts, surveys)

    • Ethics documentation & accessibility

    • Digital / AI-assisted communication governance

  • Purpose: To strengthen proposals by demonstrating that communication, dissemination, and participant-facing deliverables will be handled by an experienced, external supplier with a proven track record.

    • What this typically includes:

      • Light-touch review of draft work packages (communication, dissemination, ethics-related)

      • Alignment of planned deliverables with realistic production workflows

      • Ensuring deliverables are clearly scoped, feasible, and review-proof

      • Referencing an established portfolio and operational website to support credibility

      Why this matters to evaluators:

      • Signals that communication is not an afterthought

      • Reduces delivery risk for complex or multi-year projects

      • Reassures reviewers that specialist work will not fall to scientific staff

      Scope and limits:

      • Time-limited (typically 3–5 hours per proposal)

      • No unpaid production or open-ended consulting

      • All pre-submission input is conditional on being named or budgeted if the project is funded

  • Embedded Specialist Support: If a project is funded, communication and participant-facing deliverables are supported through a defined, embedded allocation, integrated into an existing work package.

    • Value for the consortium:

      • Communication, dissemination, and ethics deliverables are handled by a specialist team member, not absorbed by scientific staff

      • Outputs are planned and delivered in line with project milestones, reducing last-minute pressure before reviews

      • An experienced external supplier embedded in the team reduces delivery and compliance risk

    • How this is typically structured:

      • A small fractional allocation (often 0.1–0.3 FTE) over 36–48 months

      • Budgeted at a proportionate level, comparable to a small number of specialist deliverables per year

      • Clear scope, predictable costs, and low administrative overhead for the consortium

    This model provides continuity and accountability, while keeping costs transparent and aligned with project needs.

  • Typical projects:

    • EU collaborative projects (e.g. Horizon Europe)

    • National funding schemes (ANR, DFG, NIHR, etc.)

    • Multi-year clinical or population studies

    • Projects with participant recruitment or public outputs

    • Independent science communication specialist experienced with:

      • Clinical trials

      • Publicly funded research

      • Participant information & dissemination

    • See bio here.

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