Master of Science in Clinical Affairs

Us Education Consultants in Delhi | Limina Academics
Course ID
NU213
Online
No
On Campus
Yes
Duration
1 Year
Semester
Course Level
500, 600, 700

If you’re an educational professional who are looking to progress into management and consultancy, or an educational planning or development role, this is the best degree for you.

A Bachelor’s Degree from an Accredited college or University with an overall GPA of 2.5 or better,
or a GPA of 2.75 or higher achieved in the last 90 quarter units with a proficiency in english, TOEFL score of atleast a 79(IBT) or IELTS score of 6 or more

  • Cost per Quarter Unit $430
  • 4.5 unit quarter course $1989
150K ALUMNI WORLDWIDE 4 WEEK CLASSES #1 IN SAN DIEGO
Become a part of NU’s global alumni community.
The MS in Clinical Affairs program includes four-week classes.
 
National University is San Diego’s largest private nonprofit university.

In the Master of Science in Clinical Affairs (MSCA) program, you’ll gain a comprehensive understanding of the need for and the design, implementation, and management of clinical trials from a biomedical perspective. Throughout your clinical research courses, you’ll learn the global regulations, standards, and statutes required for the design, development, approval, performance, and reporting of clinical trials.

The clinical research degree program explores the latest in lectures, case studies, research, and articles associated with the global biomedical industry. Study materials include texts by regulatory and governmental agencies engaged in clinical trial research monitoring, coordination, and compliance. This program will prepare you with comprehensive knowledge of the field, the clinical life cycle, and the importance of careful data management. When you graduate, you’ll fully understand the critical role that clinical trial research plays in the development of biologic, device, and drug products, and be prepared to seek entry into this fulfilling field with confidence.

Program Learning Outcomes

Employ the global regulations, standards, and GCPs involved in designing, implementing and managing clinical trials for biologics, medical devices, and drugs.
Apply knowledge of human rights obligations, the clinical life cycle, and adverse events to the design of a clinical trial.
Select and utilize standard biomedical clinical affairs operating policies, procedures, forms, templates, reports, and electronic records.
Design a methodology for a clinical trial with supportive data management and data analysis.
Write compliance documents for clinical trials.
Conduct a clinical trial regulatory audit/inspection.