A focused 15-minute fit check — only the assessments that actually predict success in this role. No fluff, no full battery.
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Healthcare
A Clinical Research Coordinator (CRC) is the operational backbone of a clinical trial site — the person who executes the protocol on the ground while the Principal Investigator provides medical oversight. In India, CRCs work at investigator sites (AIIMS, Apollo, Manipal, KEM Mumbai, CMC Vellore, PGIMER) and for Contract Research Organisations (ICON plc India, IQVIA India, Parexel, Syneos Health, PPD/Thermo Fisher, Lambda Therapeutic Research, Veeda Clinical Research) coordinating sponsor-funded trials under ICH-GCP E6(R3) guidelines and CDSCO / DCGI regulatory requirements. Day-to-day work spans obtaining informed consent from trial participants, entering source data into Electronic Data Capture (EDC) systems like Medidata Rave or Veeva Vault, preparing for and hosting monitor visits, and ensuring Serious Adverse Events (SAEs) are reported to the IEC and DCGI within the mandatory 24-hour window. India is a top-three global destination for Phase II–IV clinical trials due to its large treatment-naive patient populations, cost efficiency, and a trained workforce — creating sustained demand for site-level CRC talent.
Tells us if the day-to-day activities of this role energize you.
Reveals whether the working style this role demands fits how you naturally show up.
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