Scale Your Clinical Workforce. Accelerate Enrollment. Strengthen Retention.

CPD-Certified Training for CROs, SMOs, Site Networks, Patient Recruitment Partners, Decentralized Trial Providers, and Organizations Entering the Clinical Research Space.
Train your CRAs, study coordinators, site managers, patient recruitment teams, and regulatory specialists on the workflows sponsors expect — CPD-certified, scalable, and delivered by a working CRO with 25+ years of collective trial experience.
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Why CROs, SMOs, and Clinical Trial Delivery Partners Choose GlobalCore

Workforce-ready credentials that accelerate site activation, enrollment, retention, and protocol compliance across global trial portfolios.
Trust-Signal
  • CPD-certified curriculum recognized across North America, GCC, Africa, and APAC
  • Built and taught by a working CRO with 25+ years of collective trial experience
  • Cohort enrollment, account-level reporting, and dedicated workforce-acceleration support
  • Aligned to ICH-GCP, sponsor SOPs, and regulatory authority expectations
  • 12 months platform access from enrollment date for every CRA, coordinator, and specialist
  • Mentoring built into every course — not just self-paced video
  • Scalable from 10-person therapeutic teams to 500-person global delivery cohorts

Our Workforce-Ready Courses

Five CPD-certified tracks. Map them directly to the specialty roles CROs, SMOs, site networks, patient recruitment partners, and decentralized trial providers hire for.

Workforce Acceleration Bundles

Combine courses to build CRA bench, accelerate site activation, strengthen recruitment and retention, and prepare delivery teams for global trial portfolios. Save when enrolling cohorts.

Who We Serve

GlobalCore builds workforce capability for the full clinical trial delivery ecosystem — from global CROs and specialized SMOs to site networks, patient recruitment partners, decentralized trial providers, and the technology vendors enabling modern trials.

Contract Research Organizations (CROs)

Global and mid-sized CROs scaling CRA bench, regulatory affairs, and clinical operations capacity to support sponsor portfolios across therapeutic areas and geographies.

Site Management Organizations (SMOs)

SMOs delivering site activation, study coordination, regulatory submissions, and patient recruitment across investigative site networks — building the workforce that drives enrollment and retention.

Trial Acceleration Companies

Site selection, feasibility, and activation platforms accelerating sponsor and CRO study startup — building the regulatory, monitoring, and coordination workforce that turns acceleration into delivery.

Patient Recruitment & Retention Partners

Digital patient recruitment specialists, pre-screening services, retention campaign providers, and diversity-focused recruitment firms training coordinators, site liaisons, and patient-facing teams on ICH-GCP, consent, and protocol-aligned engagement.

Decentralized & Hybrid Trial Providers (DCT)

DCT platforms, home health nursing networks, and direct-to-patient trial providers credentialing their mobile CRAs, virtual coordinators, and field teams on the workflows sponsors expect — ICH-GCP, consent, source documentation, and monitoring.

Site Networks & Integrated Research Organizations (IROs)

Multi-site research networks and IROs embedded in health systems building unified workforce capability across sites — coordinators, site activation leads, and regulatory specialists trained to one consistent standard.

Clinical Trial Technology & eClinical Vendors

EDC, eConsent, ePRO, and patient engagement technology providers training their implementation teams, customer success managers, and clinical liaisons on the GCP and regulatory context behind the platforms they deploy.

Organizations Entering Clinical Research

Hospital networks, digital health companies, AI healthcare startups, and adjacent service providers building credentialed teams to enter the clinical research delivery market.

In-House Sponsor Delivery Teams

Sponsors running internal clinical operations and FSP models — building their own CRA bench, regulatory specialists, and site management capability rather than outsourcing every function.

Ready to Accelerate Your Clinical Workforce?

Whether you're building a 10-person therapeutic team or a 500-person global delivery cohort, GlobalCore provides the credentials, structure, and account support to scale CRA bench, accelerate site activation, and strengthen recruitment and retention.

  • UAE

    medaffairs@deqaseharesearch.ae
    +971 58 665 3631

  • North America

    medaffairs@cradvancement.com
    +1 678 221 4098
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