Build Research Capability. Win Sponsor Trials. Retain Top Talent.

CPD-Certified Training for Clinical Trial Sites, Research Centers, Hospitals, and Academic Medical Centers — building site-level capability in study coordination, regulatory affairs, and CRC-to-CRA career advancement.
Equip your CRCs, study staff, regulatory coordinators, and PIs on the workflows sponsors expect — ICH-GCP, consent, source documentation, IRB submissions, and authority correspondence. CPD-certified, taught by a working CRO with 25+ years of collective trial experience, and built to support CRCs advancing into CRA roles.
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Why Sites, Research Centers, and Hospitals Choose GlobalCore

Site-ready credentials that strengthen study coordination, regulatory submissions, and patient enrollment — plus a clear CRC-to-CRA career pathway that helps sites retain and grow their best staff.
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
  • Site-focused workflows: consent, source documentation, IRB submissions, and monitoring readiness
  • Career pathway support — CRCs advancing into CRA roles through structured CPD certification
  • 12 months platform access from enrollment date for every coordinator, regulatory specialist, and investigator
  • Scalable from single-site PI practices to multi-hospital academic medical center networks

Our Workforce-Ready Courses

Five CPD-certified tracks. Map them directly to the roles sites, research centers, and hospitals need — from study coordinators to regulatory specialists to CRCs advancing into CRA careers.

Workforce Acceleration Bundles

Combine courses to build site-level capability, strengthen regulatory submissions, support CRC career advancement, and prepare your team for sponsor-ready trial delivery. Save when enrolling cohorts.

Who We Serve

GlobalCore builds site-level capability for the full clinical research site ecosystem — from independent investigator practices and academic medical centers to community hospitals, specialty clinics, and government health facilities running trials worldwide.

Clinical Trial Sites

Independent and private practice research sites training their CRCs, regulatory coordinators, and study staff on the workflows sponsors expect — from consent and source documentation to monitoring readiness.

Clinical Research Centers

Academic and standalone research centers building unified workforce capability across coordinators, regulatory specialists, and investigators — trained to one consistent CPD-certified standard.

Academic Medical Centers (AMCs)

University hospitals and academic medical centers training their research workforce — CRCs, IRB coordinators, regulatory specialists, and investigators leading both sponsor-led and investigator-initiated trials.

Investigator Sites & PI Practices

Physician-led practices running trials as a clinical and revenue line — oncology, dermatology, cardiology, and beyond. Training for the small site teams that need broad capability across coordination and regulatory work.

Dedicated Research Sites & Site Networks

Purpose-built research sites and multi-site networks scaling site-level capability across geographies — unified training for coordinators, regulatory specialists, and site activation leads.

Hospital Networks & Health Systems

Multi-hospital systems and integrated health networks training research workforce across facilities — building consistent capability in coordination, regulatory submissions, and protocol compliance.

Specialty Clinics & Therapeutic-Focused Sites

Oncology centers, cardiology clinics, ophthalmology practices, fertility centers, and rare disease sites — sites with deep therapeutic expertise building the research training that sponsor work requires.

Community Hospitals & Regional Medical Centers

Community hospitals and regional medical centers entering clinical research to expand patient access and support trial diversity — training a research-ready workforce from day one.

Veterans Affairs (VA) & Government Health Facilities

VA medical centers, military health facilities, and government-operated hospitals running significant trial volume — training research coordinators, regulatory liaisons, and investigators to sponsor and authority standards.

University Research Departments

Pharmacy schools, nursing schools, public health programs, and clinical research training departments equipping students and faculty with CPD-certified credentials in coordination, monitoring, and regulatory affairs.

Investigator-Initiated Trial (IIT) Groups

Academic researchers and sponsor-investigators running their own IND/CTA studies — training in GCP, regulatory submissions, and authority correspondence distinct from sponsor-led trial work.

Coordinating Centers & Cooperative Group Hubs

Central coordinating centers for multi-site cooperative groups and NIH-funded networks — unifying training across coordinators, regulatory leads, and data managers spanning dozens of participating sites.

Ready to Train Your Site Team?

Whether you're a single-investigator practice, a community hospital entering research, or a multi-site academic medical center, GlobalCore provides the credentials, structure, and account support to train CRCs, build regulatory capability, and help your best coordinators grow into CRA careers.

  • UAE

    medaffairs@deqaseharesearch.ae
    +971 58 665 3631

  • North America

    medaffairs@cradvancement.com
    +1 678 221 4098 
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