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Go from zero to a trial ready skillset: GCP, ethics, protocol design, and a full clinical trial simulation as a coordinator.
8 modules · 48 lessons
Clinical research foundations, ethics and human subject protection, ICH GCP and the regulatory framework, clinical trial design and protocol, a minor project building a study startup package, site operations and the CRC role, data management safety and monitoring, and a major project running a complete trial simulation.
Kickstart your journey into clinical research with this beginner friendly program from Ucanly, open to life sciences, pharmacy, nursing, biotechnology, medicine, dentistry, and allied health graduates with no prior research experience required. This course takes you from understanding the drug development lifecycle to running a complete clinical trial simulation as a Clinical Research Coordinator, with mentor guidance at every step. You will learn research ethics and human subject protection, ICH GCP E6 and the Indian and global regulatory framework, and clinical trial design including phases, randomization, and protocol structure. In your minor project in week five, you will build a complete study startup package including a protocol synopsis, an informed consent form, a CRF design, and an ethics committee submission dossier. You will then learn site operations, clinical data management, safety reporting, and monitoring, before your major project in week eight: a full end to end clinical trial simulation covering site activation, subject enrolment and consent, source documentation, data entry, safety reporting, monitoring visit response, and study closeout. All studies, subjects, and data used in this program are entirely simulated, and this program teaches ethical, compliant clinical research practice only.
Complete this course to earn a verified Ucanly certificate you can add to your profile, share on LinkedIn, and showcase to employers as proof of the skills you've built.
No, this course starts from absolute zero and is open to life sciences, pharmacy, nursing, biotechnology, medicine, dentistry, and allied health graduates.
No, all studies, subjects, and data used in this program are entirely simulated. This program teaches ethical, compliant clinical research practice only, and never substitutes for regulatory or medical judgement.
Yes, your major project is a full end to end clinical trial simulation run as a Clinical Research Coordinator, covering site activation through study closeout.
Yes, you will receive a Certificate of Completion from Ucanly once you finish the course, along with direction toward ICH GCP certification and ACRP and SOCRA pathways.