Clinical Research Course
OR
Prepared by Docthub Courses Team ∣
Last updated on 17 Jul 2025
Overview
The basic rules for organising, running, and managing clinical trials are taught in this course. Topics discussed include GCP compliance, protocol writing, biostatistics, and study design. The students will study data monitoring, site management, informed consent, submission to regulatory authorities, and audit readiness. The application of theory is ensured by practice in simulations and internship training for contract research organisations, hospitals, or pharmaceutical organisations. Case studies will encompass trial logistics, data collection, and safety monitoring. The course will mention patient rights and ethical review. By the end of this course, students should be coordinators across departments to start, manage, and close clinical studies. The course will mainly emphasise communication with sponsors, investigators, and IRBs, along with good documentation processes. Graduates are ready to occupy roles with various titles within the areas of protocol writing, trial management, and clinical research associate. This training offers a solid background for career development in advanced research or regulatory affairs.
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Qualifications
BSc Nursing
BPharm (Bachelor Of Pharmacy)
BSc Life Sciences
Related Specialty
Pharmacy Law and Ethics
Clinical Research Nursing