Clinical Trial Workload Assessment Survey
Please complete this survey to help us better understand the workload and responsibilities of clinical trial staff.
Your Full Name
*
First Name
Last Name
Your Role in the Clinical Trial
*
Please Select
Principal Investigator
Study Coordinator
Research Nurse
Data Manager
Regulatory Specialist
Other
How many years have you worked in clinical trials?
*
On average, how many clinical trials are you currently managing or involved in?
*
Please rate your workload in the following areas:
*
Rows
Very Low
Low
Moderate
High
Very High
Patient Recruitment
1
2
3
4
5
Data Entry & Management
6
7
8
9
10
Regulatory Documentation
11
12
13
14
15
Study Visits & Coordination
16
17
18
19
20
Reporting/Meetings
21
22
23
24
25
How would you rate the adequacy of resources provided for your work?
*
Not Adequate
1
2
3
4
Very Adequate
5
1 is Not Adequate, 5 is Very Adequate
How satisfied are you with the distribution of tasks within your team?
*
1
2
3
4
5
What are the main challenges you face in managing your clinical trial workload? (Select all that apply)
*
Insufficient Staffing
Short Deadlines
Complex Protocols
Administrative Burden
Limited Training
Other
How many hours per week do you typically dedicate to clinical trial activities?
*
Please share any suggestions for improving workload management in clinical trials.
Submit Survey
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