Our Services

Axiom Clinical Consulting helps clinical research teams deliver high-quality studies with precision, clarity, and less stress. From startup to closeout, we offer hands-on support where and when it matters most.

You do meaningful work. We’re here to support it.

Clinical research team reviewing study timelines, documents, and dashboards during a project planning session.

Project Management

Structure, support, and strategy from startup to closeout.

From study startup through closeout, we help bring clarity and control to every phase of your trial. Whether you need big-picture strategy or hands-on coordination, we step in to keep your team focused and your study on track.

Services may include:

  • Study timeline and milestone planning

  • Trial coordination and vendor/sponsor communication

  • Site support and operations tracking

  • Document management and audit readiness

  • Status reports, trackers, and oversight tools

  • Risk mitigation and action plans

Let’s tailor a plan that meets your trial’s needs and timeline.

Physician reviewing clinical trial protocols and documents on a laptop with a stethoscope on the desk.

Medical Writing & Protocol Development

Clear, compliant, and confidence-building documentation.

Your trial documents should reflect the quality of your research—accurate, aligned, and written with purpose. We support your team with regulatory-aware, reader-friendly materials that clearly communicate your science.

Documents we support include:

  • Study protocols and protocol amendments

  • Investigator brochures and site documents

  • Trial-related SOPs and workflows

  • Study tools, guides, team- and patient-facing materials

  • Final reports and publication support

Whether you're starting from scratch or refining what’s already written—we can help.

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Training & Education for Research Staff

Custom training to build clarity, confidence, and compliance

When teams understand the “why” behind what they’re doing, quality improves. We create custom training materials and sessions designed to meet your team’s needs—whether they’re new to research or ready for next-level development.

Training options may include:

  • Good Clinical Practice (GCP) fundamentals

  • Study-specific protocol and process training

  • Site management and coordinator/staff onboarding

  • Investigator and sponsor engagement tools

  • Custom team guides and SOP walk-throughs

We’ll build a training plan that makes sense for your team, your goals, and your timeline.

Who We Work With

Supporting research teams across every kind of trial environment.

We partner with clinical research teams who care deeply about quality, accuracy, and integrity—and who value having a supportive, structured partner by their side.

Clinical Trial Sites
Independent sites or site networks looking for hands-on project support, documentation help, or streamlined training.

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Academic Research Centers
University and hospital-based teams that need structure and clarity to manage complex trial portfolios.

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Small to Mid-Sized Biotech Companies
Biotech teams seeking practical, reliable support for study operations, writing, or training—tailored to their scale and therapeutic focus.

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Clinical Research Organizations (CROs)
CROs that need expert documentation, training support, or help coordinating across sponsors and sites.

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Specialized Research Teams
Groups running trials in internal medicine, oncology, rare diseases, or other focused areas—who need experienced, reliable partners.

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Every client—and every trial—is unique. We meet you where you are, helping you manage your studies with clarity, confidence, and consistency.