Vilo Research Group

About

About the Program

CRC Training Hub · January 2026 · v2026.1

Our Mission

The CRC Training Hub exists to make rigorous, internationally-aligned training for Clinical Research Coordinators accessible to professionals worldwide. We combine current regulatory standards, real-world site operations, and interactive assessments so learners build the practical competencies that sponsors, CROs, and IRBs expect.

Standards-Aligned

Curriculum follows TransCelerate BioPharma minimum criteria for ICH-GCP investigator site personnel training and the ICH-GCP E6(R3) guideline.

Practice-Based

80 CPD hours of lessons, scenario-based quizzes (80% pass), case studies, and downloadable checklists.

Verifiable Certificate

Each certificate carries a unique verification code, CPD hours, issue date, and the standards-alignment statement.

For Working CRCs

Built around the daily workflow: protocol management, source documentation, AE/SAE reporting, IATA shipping, EDC/eTMF, and audit readiness.

Methodology

  • · Self-paced learning with measurable objectives at every module.
  • · Scenario-based assessments with immediate feedback and explanations.
  • · Real case studies reflecting common site situations: deviations, AE reporting, audits, IATA incidents.
  • · Glossary with 80+ key clinical research terms.
  • · Final integrative exam required for certification.
  • · Annual content review to maintain alignment with current regulations.

Statement on TransCelerate BioPharma

This course is updated to ICH E6(R3) and covers the key principles of Good Clinical Practice (GCP) per the International Council for Harmonisation guideline. The GCP module is designed in alignment with the Minimum Criteria for ICH E6(R3) GCP Investigator Site Personnel Training established by TransCelerate BioPharma.

Important: this integral training program for Clinical Research Coordinators (CRC) does not substitute a specific GCP course listed in the TransCelerate Mutual Recognition program. However, it solidly prepares participants to meet the GCP requirements expected by most pharmaceutical sponsors and facilitates the site qualification process. We recommend complementing this course with a sponsor-recognized GCP training (such as CITI Program, PharmaEduCenter or others officially listed) according to each sponsor's policies.

Statement on TransCelerate BioPharma

This course is updated to ICH E6(R3) and covers the key principles of Good Clinical Practice (GCP) per the International Council for Harmonisation guideline. The GCP module is designed in alignment with the Minimum Criteria for ICH E6(R3) GCP Investigator Site Personnel Training established by TransCelerate BioPharma.

Important: this integral training program for Clinical Research Coordinators (CRC) does not substitute a specific GCP course listed in the TransCelerate Mutual Recognition program. However, it solidly prepares participants to meet the GCP requirements expected by most pharmaceutical sponsors and facilitates the site qualification process. We recommend complementing this course with a sponsor-recognized GCP training (such as CITI Program, PharmaEduCenter or others officially listed) according to each sponsor's policies.

Important Disclosure

This is a continuing professional development (CPD) course. The certificate of completion does not replace external professional credentials such as ACRP CCRC, SOCRA CCRP, PRCCI, CCRPS, or university-issued diplomas, which require separate eligibility, examinations, and fees. The CRC Training Hub prepares you for those credentials but is not affiliated with their issuing bodies.