The Master of Science in Clinical Research Organization and Management, offered by TAU is a 60 credit program in which the student is also required to bring out research paper with Dissertation and thesis
The program is tailor-made for today's busy physicians, physician assistants, nurses, clinical fellows, research coordinators, and individuals working in the field.
As the clinical research field expands and evolves, so too does the increased need for highly trained and qualified research professionals encompassing all research and regulatory areas. This program allows students to earn the experience and knowledge necessary to conduct investigations in the increasingly complex and highly regulated clinical research field, and introduces students to timely and contemporary industry-related issues.
Key Program Features and Benefits:
> Well-rounded curriculum combining 5 tracks of study: New Product Research, Regulatory Compliance and Law, Biostatistics and Data Management, Clinical Research Management and Safety & Surveillance, and Business and Strategic Planning of New Product Development.
> Unique education program: Curriculum that combines business principles, an understanding of the medical sciences pertinent to the research industry, and skills necessary for navigating the changing political, regulatory, and financial landscapes in the pharmaceutical and healthcare industries.
> Competent faculty: Curriculum designed and taught by outstanding teachers - among them experienced faculty, researchers, administrators, lawyers, and scientists working in the area of clinical research.
> Highly interactive, e-Learning system engages students while remaining convenient for the working professional.
Holders in Bachelors of Health Science subjects, Life Science subjects and Clinical related subjects
The program is OFFERED as Trimester program [ 3 semesters a year]. The student can finish the program in Less than 18 months
S No |
COURSES |
SEMESTERS |
|||
I |
II |
III |
IV |
||
1 |
Pharmacology and Pharmacotherpeutics-I |
3 |
|
|
15 (Research & Thesis Paper) |
2 |
Pharmacology and Pharmacotherpeutics-II |
|
3 |
|
|
3 |
Drug Discovery Development |
2 |
|
|
|
4 |
Biomedical Basis of Diseases |
|
|
3 |
|
5 |
Biostatistics |
|
1 |
|
|
6 |
Introduction to Clinical Trials |
2 |
|
|
|
7 |
Principle of Practice of Clinical Trials |
3 |
2 |
|
|
8 |
Regulatory Affairs in Clinical Trials |
|
2 |
|
|
9 |
Ethical Aspects in Clinical Trials |
|
2 |
|
|
10 |
Clinical Data Management |
|
3 |
|
|
11 |
Pharmacovigilance |
|
1 |
|
|
12 |
Quality Control and Audit in Clinical Trials |
|
|
2 |
|
13 |
GCP/GCP in Clinical Trials |
|
|
2 |
|
14 |
Communication Skills |
|
|
2 |
|
15 |
Medical Writing / Reporting |
|
|
2 |
|
16 |
Intellectual and Property Rights |
|
|
2 |
|
17 |
Statistical Analysis Software (SAS) |
2 |
|
|
|
18 |
Seminar in Clinical Research |
1 |
1 |
1 |
|
19 |
Assignments in Clinical Research |
2 |
1 |
1 |
|
TOTAL CREDITS |
|
15 |
15 |
15 |
15 |