Study Coordinator

Study Coordinator performs essential activities towards the successful execution of clinical research. Study coordinators are tasked with an expanding set of responsibilities including patient safety and recordkeeping, federal regulations compliance, IRB compliance, interacting with Sponsors and Clinical Research Organizations and dealing with the budget and contract negotiation.


Clinical Research Associate (CRA)

Clinical Research Associate Course is designed for persons with or without prior on-site clinical trials experience, seeking qualifications and/or current practical knowledge to effectively work as a Principal Investigator (PI), Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Coordinator or Clinical Data Manager (CDM) in the monitoring of clinical trials globally in all countries that follow the ICH-GCP guidelines for conducting clinical trials.

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