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M410- Clinical Research Study Management and Compliance (CRSMC) Course CTCR Masters- Fall 2025
1.
The course objectives and faculty expectations of the scholars were clearly defined?
Yes, completely
Yes, mostly
Yes, partially
No
2.
The course syllabus was
Excellent
Very good
Good
Fair
Poor
3.
Overall, the format of the class was effective in helping meet the course objectives
Yes, completely
Yes, mostly
Yes, partially
No
4.
The course helped you towards your goal of improving your ability to conduct successful clinical and translational research
Yes, completely
Yes, mostly
Yes, partially
No
5.
How would you evaluate the level of instruction from the course faculty?
Excellent
Very good
Good
Fair
Poor
6.
Overall, the course instructors were responsive to my needs
Yes, completely
Yes, mostly
Yes, partially
No
7.
The topics covered in the course stimulated my interest in the subject matter
Yes, completely
Yes, mostly
Yes, partially
No
8.
The topics covered in the course were
Too difficult
Somewhat difficult
Just right
Easy
Too easy
9.
The amount of work/effort required was
Too much
Enough
Not enough
10.
Score the following lectures in terms of their effectiveness in teaching the practical aspects of running clinical trials (1 – not effective, 5 very effective)
1- Not effective
2
3
4
5- Very Effective
N/A
Week 1: Introduction to Clinical Research Implementation and Management
1- Not effective
2
3
4
5- Very Effective
N/A
Week 2: Human Subjects Protection
1- Not effective
2
3
4
5- Very Effective
N/A
Week 3: The Scientific Protocol Review Process at MSK and other NCI Designated Cancer Centers
1- Not effective
2
3
4
5- Very Effective
N/A
Week 4: INDC and DSMC
1- Not effective
2
3
4
5- Very Effective
N/A
Week 7: Sponsor – Investigator Relationships and Responsibilities
1- Not effective
2
3
4
5- Very Effective
N/A
Week 8: The Patient’s Perspective
1- Not effective
2
3
4
5- Very Effective
N/A
Week 9: Securing Multidisciplinary Support and Multimodality Studies
1- Not effective
2
3
4
5- Very Effective
N/A
Week 10: Conduct of the Trial Part I
1- Not effective
2
3
4
5- Very Effective
N/A
Week 11: Conduct of the Trial Part II
1- Not effective
2
3
4
5- Very Effective
N/A
Week 12: Multicenter Trials
1- Not effective
2
3
4
5- Very Effective
N/A
Week 13: Effective Documentation and Corrective and Preventive Action Plan Reviews
1- Not effective
2
3
4
5- Very Effective
N/A
Week 14: Financial Accountability
1- Not effective
2
3
4
5- Very Effective
N/A
Week 15: FDA Regulations
1- Not effective
2
3
4
5- Very Effective
N/A
11.
What aspects of the course were strongest?
12.
What aspects of the course would you improve?
13.
What additional topics should this course cover?
14.
Please provide any additional recommendations or comments below.