In the past 12 months, have you worked on clinical trials at your site?
What is your primary role in clinical trials at your site?
- Principal Investigator (PI)
- Sub-Investigator
- Study Coordinator/CRC
- Research Nurse
- Data Manager
- Pharmacist
- Other
How many interventional trials did you actively support in the past 30 days?
Outside of trials, about how many hours per week did you spend on clinical documentation and data entry in the past 30 days?
Overall, how burdensome was non‑trial clinical documentation in the past 30 days?
Which systems took most of your non‑trial documentation time in the past 30 days? Select all that apply.
- EHR
- Quality registry portals
- Prior authorization portals
- Spreadsheets
- Paper forms
- Other
What was the biggest barrier to efficient non‑trial documentation in the past 30 days?
Max 600 chars
On average, how many hours per week did you spend on trial documentation and data entry in the past 30 days?
Overall, how burdensome was trial data capture at your site in the past 30 days?
Which tools did you use for trial data capture in the past 30 days? Select all that apply.
- Sponsor-specific EDC
- eSource platform
- EHR-to-EDC integration
- Paper source
- Spreadsheets (e.g., Excel)
- Other
Which was your primary system for entering trial data in the past 30 days?
For your primary digital system, how easy or difficult were these tasks in the past 30 days?
Overall, how satisfied are you with your primary system for trial data entry?
Rank up to 3 of your biggest trial data capture pain points (1 = biggest).
Allocate 100 points across these trial activities to reflect your time in the past 30 days (must total 100).
What one change would most reduce trial data capture burden at your site?
Max 600 chars
How confident are you that your site can meet sponsor data timelines over the next 3 months?
What type of site do you primarily work at?
- Academic medical center
- Community hospital
- Private practice
- Independent research site/SMO
- FQHC/Public clinic
- Other
How many years have you worked in clinical research (any role)?
What patient population do you primarily serve?
Which trial phases do you typically support? Select all that apply.
- Phase I
- Phase II
- Phase III
- Phase IV/Post-market
- Medical device studies
- Other
Country/region where you primarily work:
Max 600 chars
Attention check: To confirm attention, please select "No."
Any additional comments about site documentation or data capture in the past 30 days?
Max 600 chars
AI Interview: 2 Follow-up Questions on Trial Documentation and Data Capture
Thank you for your time—your input will help reduce site burden and improve data capture workflows.