Global Clinical Research & Regulatory Training for Every Stage of Your Career
Why GLOBALCORE™?
Most “global” training is fragmented or focused on a single region. GLOBALCORE™ is built from the ground up as a truly international institute, serving individuals and organizations across multiple continents.
Created by a global full‑service CRO with multi‑region clinical trial experience.
Backed by 25+ years of clinical research and regulatory expertise.
Combines ICH‑GCP and international regulatory standards with practical, role‑based training for modern clinical teams.
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Monitoring & Closeout
Utilizing advanced monitoring techniques, we maintain high data quality. Our Comprehensive trial closeout services include data cleaning, monitoring, and reporting
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Recruitment & Retention
Equipped with patient-centric recruitment strategies, digital technologies, real-world data, and decentralized trial solutions, we boost enrollment and retention globally.
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New to Clinical Research
Step into clinical research with a clear, structured path designed for recent graduates, early-career professionals, and those new to the industry.
Find the Right Pathway for You
Built for Global CPD and Real-World Impact
CPD-ready
Clear learning objectives, mapped hours, and structured assessments
Globally relevant
Aligned with ICH-GCP and international best practices
Globally relevant
Aligned with ICH-GCP and international best practices
Practice-oriented
Case studies, checklists, templates, and tools that translate to day-to-day work
Practice-oriented
Case studies, checklists, templates, and tools that translate to day-to-day work
Quality-assured
Annual content review synchronized with ICH-GCP and regulatory updates
Quality-assured
Annual content review synchronized with ICH-GCP and regulatory updates
Core Programs
- 40 CPD hours, self-paced with optional live Q&A.
- ICH-GCP and global regulatory foundations.
- Feasibility, start-up, on-site and remote monitoring, and close-out.
- Risk-based monitoring, SDV/SDR, protocol deviations and CAPA.
- TMF expectations and inspection readiness.
- Professional communication and career advancement strategies.
- Ideal for: Junior to mid-level CRAs, experienced CRCs/CTAs, research pharmacists and nurses.
CRA Professional Certification
Outcome: Practice-ready CRAs who can monitor complex multi-country trials.
- 30 CPD hours, self-paced with optional live case walkthroughs.
- CRC role across the full study lifecycle.
- Participant recruitment, screening, informed consent, and visit management.
- Source documentation and EDC data entry quality.
- AE/SAE reporting, deviation management, and working with CRAs.
- Preparing for monitoring visits, audits, and regulatory inspections.
- Ideal for: Site coordinators, research nurses, site pharmacists, new site staff.
CRC / Site Study Coordinator Certification
Outcome: High-performing CRCs who drive recruitment, data quality, and inspection readiness.
- Designed for newcomers to RA, experienced RA specialists, and organizations building RA capability.
- Regulatory Affairs – Global Foundations
- Regulatory Affairs – GCC Regulatory Guidelines & Africa (Regional Expert Track)
- 45 CPD hours for Regional Expert Track
- Self-paced with recorded regulator simulations
Regulatory Affairs Pathway
A two-level RA pathway to support global and regional strategy.
Delivery Models & Pricing
Get Started with GLOBALCORE™
Whether you are enrolling as an individual or designing training for a team, we help you map the right program pathway, cohort structure, and CPD approach.
Share your priorities
Target roles (CRA, CRC, RA) and regions.
We design your academy
Programs, cohorts, timelines, and CPD approach.
Launch your first cohort
With clear competency goals and measurable outcomes.