Clinical Trials Management
Clinical trials managers are involved in numerous aspects of research, including data collection, analysis, and monitoring.
Working in medical or educational institutions, as well as research laboratories, often requires managing a clinical trial. Clinical Trials Managers oversee all aspects of the trial, including patient recruitment, study implementation, and close out. This program will provide learners with the skills needed to contribute to positive changes within the medical field.
Duration: One year, full time | September to August
Program: 9 required courses and one, 400-hour practicum
Note: International Students will pay $6800, ancillary fees and UHIP (University Health Insurance Plan).
Clinical Trials Management is a one-year, full-time program, combining eight months of learning online (Sept-April) and four months in a practicum placement (May-Aug).
To pursue a Post-Degree Diploma you need to apply.
The nine required courses are taught and developed by industry professionals to connect theory to practice. You will develop a professional network, unique skills, and a portfolio of projects used throughout your career.
What you will learn
Learn the historical background of the laws governing drug development (FDA Regulations)
Possess a strong understanding of key regulations that impact the development of drugs
Differentiate the types of clinical trial designs
Know the terminology and definitions used in clinical trials the laws that govern the drug approval process
abilityanalyze and interpret safety and efficacy data
Develop strategies for organizing clinical trials and site management to ensure a successful outcome of the trial
Learn the principles of ICH GCP responsibilities in the clinical trial process
Through the practicum, you will gain valuable hands-on experience, a strong network of industry contacts, and an edge in the job search process. It is the culmination of your work in the classroom and the bridge to a great career in your target industry