claude

clinical-trials

Clinical Trials specialist team — agents, skills, cited knowledge bank, templates, commands, best-practice rules, an advisory hook. A clinical-operations team for a sponsor, CRO, or site network — it designs feasible protocols (because eligibility criteria drive the enrollment failure that hits two-thirds of sites), plans patient recruitment against a ~$6,533 per-patient cost (and ~$19,533 to replace), manages site activation and the ~30% dropout, and frames the regulatory submission the way a study where 80% run late demands. Inherits ravenclaude-core protocols.

9 on GitHubby Matt Corbettv0.3.4MITupdated today
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Plugin clinical-trials from marketplace ravenclaude in mcorbett51090/RavenClaude. Commands read from the repo's manifest — today.

This plugin runs code on your machine — its hooks fire automatically on events like tool use. The exact commands are listed below; read them before installing.

What it installs

Skills (5)

  • accelerate-site-activation

    Sequence site selection, contracting, and start-up as the schedule's critical path to cut the activation delay. Reach for this when sites are slow.

  • design-for-retention

    Build retention into visit burden, schedule, and engagement to lower the ~30% dropout, instead of re-recruiting. Reach for this when dropout threatens the timeline.

  • plan-recruitment-funnel

    Plan recruitment as a costed funnel with a cost per stage, against the per-patient economics, instead of a hope. Reach for this on any enrollment plan.

  • read-submission-readiness

    Read documentation completeness, data quality, and eCTD structure throughout the trial so the filing isn't a final-month scramble. Reach for this before a milestone.

  • stress-test-feasibility

    Stress-test eligibility criteria against the addressable population and site capacity before the protocol locks, since restrictive criteria are the biggest enrollment killer. Reach for this at design.

Slash commands (5)

  • /clinical-trials:accelerate-site-activation

    Sequence site selection, contracting, and start-up as the schedule's critical path to cut the activation delay. Reach for this when sites are slow.

  • /clinical-trials:design-for-retention

    Build retention into visit burden, schedule, and engagement to lower the ~30% dropout, instead of re-recruiting. Reach for this when dropout threatens the timeline.

  • /clinical-trials:plan-the-recruitment-funnel

    Plan recruitment as a costed funnel with a cost per stage, against the per-patient economics, instead of a hope. Reach for this on any enrollment plan.

  • /clinical-trials:read-submission-readiness

    Read documentation completeness, data quality, and eCTD structure throughout the trial so the filing isn't a final-month scramble. Reach for this before a milestone.

  • /clinical-trials:stress-test-protocol-feasibility

    Stress-test eligibility criteria against the addressable population and site capacity before the protocol locks, since restrictive criteria are the biggest enrollment killer. Reach for this at design.

Subagents (4)

  • clinical-operations-manager

    Use this agent for trial execution — site activation, the recruitment funnel, monitoring, and retention operations. NOT for protocol design (route to protocol-design-specialist) or submission assembly (route to regulatory-submissions-specialist).

  • protocol-design-specialist

    Use this agent for protocol feasibility — eligibility, enrollment risk, and retention-by-design, as medical-team decision-support. NOT for medical/safety decisions (the medical team's) or recruitment execution (route to clinical-operations-manager).

  • regulatory-submissions-specialist

    Use this agent for regulatory submissions — documentation, eCTD structure, data quality, and readiness, as regulatory decision-support. NOT for regulatory/medical decisions (the qualified lead's) or recruitment (route to clinical-operations-manager).

  • trials-engagement-lead

    Use this agent to scope a clinical-operations problem, frame a feasibility review, or route to a specialist. The orchestrator. NOT for the protocol design detail (route to protocol-design-specialist) or submission structure (route to regulatory-submissions-specialist).

Hooks (1)

  • PostToolUse

    /usr/bin/env -u BASH_ENV -u ENV -u SHELLOPTS -u BASHOPTS -u LD_PRELOAD -u LD_LIBRARY_PATH -u LD_AUDIT -u DYLD_INSERT_LIBRARIES -u DYLD_LIBRARY_PATH -u PYTHONPATH -u PYTHONSTARTUP PATH=/usr/local/bin:/

View source on GitHub mcorbett51090.github.io

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