Level 1: Foundations
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Clinical trial phases, study purpose
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Sponsor, CRO, PI, CRC, CRA/monitor, IRB, and vendor roles
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Recruitment, pre-screening, and eligibility criteria
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Informed consent, audit readiness
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Screening, randomization visit workflows
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Source documentation, ALCOA, EDC basics, and regulatory expectations
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Real-world coordinator scenarios and practical checklists
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4 Weeks | Self-Paced Online
Investment: $3,000
Your Path to Becoming a Clinical Research Coordinator
From foundational knowledge → to real clinical trial experience
“Where theory becomes practice — and experience becomes opportunity.”
Level 2: Hands-On Observership
8 Weeks | Hybrid Training
Level 1: Foundations, self paced online tutorial (4 weeks)
Build real-world skills through guided scenarios (Onsite - 4 weeks):
• Informed consent
• Delegation of authority logs
• Regulatory documentation
• Adverse event reporting
• EDC & CTMS systems
Investment: $8,000 (Includes Level 1)
Level 3: Clinical Trial Experience
3, 6, or 9 Months | In-Person
Level 1: Foundations, self paced online tutorial (4 weeks)
Level 2: Hands on Observation (4 weeks)
Level 3: Work directly on active clinical trials with real patients. Perform study visits and documentation alongside experienced teams.
Investment: $12,000
(Includes Levels 1 & 2)
4
Weeks
Basic CRC course includes online, self-guided tutorials
Hybrid
Format
Level 2 and 3 CRC training combines self-paced lectures with clinical exposure at active clinical research sites.
10-12
Cohort Size
Small, selective groups ensure high-quality mentorship and meaningful clinical exposure for every student.
Weeks 1–4: Foundations
Foundational Training
Deep dive into clinical research ethics, regulatory frameworks, and the anatomy of clinical trial design through web-based, self-paced training modules
Case-Based Learning
Apply theoretical knowledge to real-world scenarios through case-based discussions
Weeks 6–11: Practicum
On-Site Exposure
Gain hands-on experience in active clinical studies, alongside experienced investigators and clinical research coordinators
Week 12: Evaluation
Competency Review
Final assessment of clinical trial documentation and workflow understanding to ensure readiness for the next phase of your career.
Learning Outcomes
We bridge the gap between academic theory and clinical practice, ensuring you gain the specific competencies required for a successful career in clinical research.
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Clinical Trial Fundamentals
Master the core principles of clinical research ethics, GCP standards, and regulatory frameworks through self-paced online video tutorials.
Patient Workflow Mastery
Gain hands-on experience navigating patient recruitment, screening, and informed consent processes.
Documentation & Compliance
Learn to maintain accurate electronic data capture and clinical trial documentation in real-time.
Site Operations & Safety
Understand the critical infrastructure and safety protocols that ensure high-quality clinical research.