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Department of Clinical Sciences
SAINT Survey
Name:
Job Title:
Degree:
_____________________________________________________________________________
Clinical or translational patient oriented research is the full or partial focus of my current position.
(Please complete remainder of survey and submit.)

My position is focused on basic or bench research, not clinical research. (Please submit without completing remainder of survey.)


My position has no research responsibilities at all.
(Please submit without completing remainder of survey.)



_____________________________________________________________________________
In your current position, how many years have you worked in clinical research?



How many years have you been involved in clinical research?



What is your highest level of completed education?



What formal training have you had in clinical research? ( Check all that apply. )



Association of Clinical Research Professionals (ACRP)

Are you currently a member of:



Society of Clinical Research Associates (SoCRA)

Certified Clinical Research Coordinator (CCRC) through ACRP

Are you currently certified in clinical research?



Certified Clinical Research Associate (CCRA) through ACRP

Certified Clinical Research Professional (CCRP) through SoCRA

Other

What kind of study trial experience do you have? ( Check all that apply. )



Which of the following tasks is part of your routine job responsibilities?


Evaluation of protocols for feasibility

Study site preparation/initiation

Patient screening

Patient recruitment

Patient enrollment

Conducting study visits

Specimen collection and handling

Accountability for maintaining and dispensing study drug

Accountability for study device

Case report form (CRF) completion

Maintaining source documents

Managing, monitoring, and editing site CRF data

IRB submission (prepare study protocol, project summary, consent form)

IND/IDE application preparation

Assist with study grant, contract, or budget

Preparation of patient education information (brochures, flyers)

Communication with IRB (study submissions, CR, modifications)

Communication with sponsor

Reporting AE/SAEs

Submission of FDA MedWatch notifications

Preparation for FDA audits

Database management

Data compilation

Data entry

Data analysis

Medical chart reviews

Quality assurance

Publications (co-authored peer-reviewed journal, chapter, or book)

Study closure procedures

How many?

Other

Regulatory oversight