Clinical Trials Management

Final Application Deadline:

Program Begins:

Program Description

  • Our Clinical Trials Management educational program provides individuals with the skills to master the procedures and administration of the clinical trials process, giving them the tools they need to lead clinical research studies.
  • Our internationally accredited program encompasses good clinical practice guidelines, regulatory requirements and compliance, and trial management.
  • Those who complete our program will be able to initiate clinical research studies, apply monitoring methods, and write exemplary documents and reports,

More Than A Program

  • Receive International Accreditation & Be Job Ready
  • On successful completion of this program, you will have acquired knowledge, skills and competencies to start at an entry level role as Clinical Research Associate, In- House Clinical Research Associate or similar.

Targeted Audience

  • Our program is designed for early or mid-career professionals with an interest in clinical research and who desire a career in regulatory compliance, trial management, or data analysis in the pharmaceutical industry, at a clinical research organization, or academic institution.

Online Course Structure

  • Our structure enables you to complete this program while you are working full-time as 100% of the program is online and the weekly training courses can be completed at any time during the week.
  • All online courses incorporate self-study activities in Moodle, our learning management system
  • The weekly, self-paced learning and materials are time-sensitive and must be completed within required timeframes
  • Synchronous sessions are conducted through Zoom

Course Fees:

2400 Egyptian Pounds

The course fees include:

  • registration fee
  • all online-training course material
  • one-year online access to our learning management system
  • exams during the training to test your knowledge
  • personalized attendance confirmation upon completion

To obtain more information:

Please completing the form below: