Vilo Research Group
CRC training program

Become a Clinical Research Coordinator You Can Count On

Practical, GCP-aligned training for people entering clinical research—structured for real site work, built around ICH E6(R3) expectations, and designed to earn trust in interviews and on the floor.

60–80 Hours6 ModulesCertificate

Already enrolled? Access your course here.

Clinical research professional reviewing documentation

TransCelerate

GCP themes mapped to sponsor criteria.

ICH E6(R3)

Documentation aligned to current GCP.

Certificate

Professional completion you can share.

What you walk away with

Outcomes you can explain in an interview—not a slide deck of buzzwords.

    GCP credibility

    Speak to monitoring questions with language sponsors recognize.

    Practice-first skills

    Cases and checks that mirror coordination decisions on site.

    Proof of completion

    A certificate you can share with employers and study teams.

Why this program

Built for aspiring CRCs who need structured training—not generic compliance theatre.

  1. 01

    Aligned to how sponsors frame training

    GCP organized with TransCelerate minimum criteria in mind.

  2. 02

    Site logistics literacy, not jargon

    Specimen handling and courier context you can use with labs.

  3. 03

    One arc across six modules

    Foundations through monitoring readiness—focused and paced.

Curriculum

Six modules · roughly 60–80 hours · learn in order or revisit sections as needed.

  • 01

    Foundations & CRC role

    How sites run and where you add value.

  • 02

    GCP & ICH E6(R3)

    Documentation and quality that hold up to scrutiny.

  • 03

    Start-up & operations

    Systems, supplies, day-to-day coordination.

  • 04

    Consent & safety

    Participant pathway and reporting essentials.

  • 05

    Biospecimens & IATA

    Chain of custody and shipping basics.

  • 06

    Monitoring readiness

    Queries, professionalism, sponsor touchpoints.

Standards & trust

  • 60–80 Hours

    Structured pacing with room for practice.

  • 6 Modules

    One coherent path from foundations to readiness.

  • ICH E6(R3)

    GCP themes aligned to current regulatory text.

  • TransCelerate

    Mapped to sponsor-style minimum training criteria.

FAQ

Who is this for?

Aspiring CRCs, career changers, and site staff who need structured GCP training—not a one-off slideshow.

How long does it take?

Plan about 60–80 hours across six modules, practice, and assessments. Go at your own pace.

What do I receive when I finish?

A professional digital certificate you can share with employers and sponsors, plus downloadable materials.

I already paid—where is the course?

Use “Access course” to open the learning app. Same link appears in the hero and at the bottom of this page.

Is this my employer’s official SOP training?

No. This is independent education. Always follow your site’s SOPs and local regulations at work.

Already enrolled?

Access your course here — same credentials as your enrollment email.

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Ready to start?

Join structured CRC training trusted by professionals entering clinical research.

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Already enrolled? Access your course here.

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