The complete, practical CRC program — from study startup to audit readiness — for freshers and working coordinators.
one-time · lifetime
The Clinical Research Coordinator (CRC) is the engine room of a trial site. The CRC manages day-to-day study conduct: consenting participants, scheduling and running visits, capturing source data, handling the investigational product, reporting safety events and hosting monitors. It is the most common entry role into clinical research and one of the most in-demand.
This program is built for real site work. It takes you from how a study starts at a site, through consent, source documentation, recruitment, study visits and safety reporting, to how you keep the site inspection-ready. It assumes no prior experience and is equally useful for working coordinators who want to fill gaps.
Complete the modules and the final exam to earn a certificate you can show employers — and walk into a site able to contribute from day one.
The CRC Role & the Trial Team, What a CRC actually does, how the role differs from a CRA and PI, and the workflow you'll live in.
Study Startup at the Site, Feasibility, regulatory and EC submissions, and the site initiation visit that lets enrolment begin.
Informed Consent in Practice, Running the consent conversation, re-consent, and avoiding the consent errors inspectors look for.
Source Documentation & Data Management, ALCOA+ source records, EDC and query resolution, and documenting protocol deviations.
Recruitment, Visits & Investigational Product
Safety Reporting, Monitoring & Audit Readiness, Reporting AEs/SAEs from the site, surviving monitoring visits, and staying inspection-ready.
CRC vs CRA vs PI: who does what
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The clinical trial workflow
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Feasibility and site selection
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Regulatory and Ethics Committee submissions
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The Site Initiation Visit (SIV)
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Conducting the consent discussion
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Re-consent and ongoing consent
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Common consent errors to avoid
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Source documents and ALCOA+
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EDC, CRFs and query resolution
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Protocol deviations and how to document them
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Recruitment and retention
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Conducting study visits
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Investigational product handling
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AE and SAE reporting from the site
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Monitoring visits: what the CRA checks
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Inspection readiness for coordinators
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6 modules · 18 lessons · Preview lessons are free to read; enroll to unlock the full course.
Clins Research Training Academy
Clins Research Pvt Ltd is a Clinical Research Site Management Organization (SMO) based in Greater Noida. Our courses are designed and delivered by practitioners with hands-on experience across the clinical trial lifecycle.
