By Successful Completion of the Master’s program in Clinical Research and Experimental Medicine, students will be skilled enough to:

• Plan and coordinate the initiation of research study protocol, and the establishment of operating policies and procedures.

• Plan, implement, and maintain data collection and analysis systems in support of research protocol

• Obtaining informed consent

• Supervise and coordinate the provision of support services to investigators and researcher

• Monitor the progress of research activities; develop and maintain records of research

• activities, and prepare periodic and ad hoc reports, as required by investigators, administrators, funding agencies, and/or regulatory bodies.

• Recording and reporting adverse reactions received from healthcare professionals and consumers.

• Writing and reviewing serious adverse effects reports and forms

• Working on clinical trials of new drugs.

• Perform continuing Professional Education and uphold legal and ethical behavior in his/her career.