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This is the first step to understanding the various facets of the clinical research industry. Understanding the Drug Development Process and grasp the importance of Good Clinical Practices (GCP) & to understand the roles and responsibilities of a clinical research team. Reporting audit queries by citing evidence of work. This will establish your role as a clinical research associate in the Industry. You will understand the different regulatory bodies and their common and uncommon ethical practices. DURATION : 4 Months -
Certified Clinical Research Coordinator
Understand the concept of Clinical Research / Trials. Understand Medical Writing and Patient Safety Management. Understand Regulatory affairs and Data Management. Understanding the Drug Development Process and grasp the importance of Good Clinical Practices (GCP) & to understand the roles and responsibilities of a clinical research team. DURATION : 3 Months -
Professional Cloud Administrator
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