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Surveys
2010
April
F
Final-Site Satisfaction Survey 2010
Final-Site Satisfaction Survey 2010
0%
Exit Survey »
Dear clinical research collaborator:
You have recently been involved or are presently involved in a Teva clinical trial and as such, we would like to get your feedback on the Teva Clinical Research Team.
Our group is constantly striving to improve the quality of its work and would appreciate it if you would take approximately
5 minutes
of your time to complete the attached questionnaire. The results will be used to enhance our collaborative research efforts.
Your survey responses will be coded and will remain
strictly confidential
. Data from this survey will be reported only in aggregate results.
We sincerely appreciate your time in completing this survey!
*
Please indicate in which Teva study/studies you have been involved in:
MS-LAQ-301 + extension (ALLEGRO – Laquinimod Placebo-Controlled)
MS-LAQ-302 + extension (BRAVO – Laquinimod vs Avonex/Placebo)
LAQ-5063 (Laquinimod in MS Phase II Open-Label Extension)
LAQ Maximum Tolerated Dose (101)
GA / 9010 - Precise – MS (CIS)
PM030 – Octagon - Acute Optic Neuritis - MS
TVP-1012/501 (ADAGIO Extension – Rasagiline Disease Modification)
MSA-RAS-202 (Rasagiline for MSA)
ALS-TAL-201 + extension (ALSTAR – Talampanel in ALS)
CD-LAQ-201 (Laquinimod for Crohn’s Disease)
EXCEL (Gamida cell- StemEx)
DR-105-101 (Seasonique & Ovulation Inhibition)
DR-105-201 (Seasonique & Menstrually Related Migraine)
DR-105-202 (Adolescent Bone Mineral Density)
DR-103-301 (Pregnancy Prevention)
DR-OXY-301 / 302 (Oxybutynin Vaginal Ring & Overactive Bladder / Urge Incontinence)
DR-PGN-302 (Progesterone Vaginal Ring & In vitro Fertilization)
DR-201-102 (Projesterone Tissue Assay)
ABS-AS-101 (Albuterol Spiromax – Asthma)
ABS-AS-201 (Albuterols Spiromax – Asthma)
*
Please indicate your role in the study:
Principal Investigator
Sub-Investigator
Study Coordinator
Study Nurse
*
How many years of experience do you have in clinical research?
-- Select --
< 1 year
1 – 3 years
3 – 5 years
> 5 years
*
Please indicate your country:
-- Select --
Argentina
Benelux
Canada
France
Germany
Hungary
Italy
Israel
Spain
UK
USA
*
Overall, how satisfied are you with the Teva Research Team?
Very Dissatisfied
Not Satisfied
Neutral
Satisfied
Very Satisfied
Please rate your satisfaction with the quality of general project management and support offered by the Teva Research Team.
Very Dissatisfied
Not Satisfied
Neutral
Satisfied
Very Satisfied
N/A
*
a) Budget/Contract Negotiation & Approval Process
*
b) Patient recruitment goals
*
c) Informed Consent Form Review & Approval Process
*
d) Support in answering the Ethics Committee/Institutional Review Board’s questions
*
e) Support with study start-up activities (eg. certifications, MRI dummy-run scans, etc.)
*
f) Training on protocol & trial-specific topics/systems
*
g) Supply of trial-specific tools (eg. charts; pocket cards, etc.)
*
h) Assistance with patient enrollment (eg. recruitment tools/material)
*
i) Timeliness of payments
j) Investigators meeting planning / training
Please rate your satisfaction with the attitude and work style of the Teva Research Team.
Very Dissatisfied
Not Satisfied
Neutral
Satisfied
Very Satisfied
N/A
*
a) Establishment of a collaborative relationship
*
b) Responsiveness to questions or concerns
*
c) Completeness of problem resolution
Please rate your satisfaction with the professionalism and expertise of the Teva Research Team.
Very Dissatisfied
Not Satisfied
Neutral
Satisfied
Very Satisfied
N/A
*
a) Site management skills and experience
*
b) Protocol and study drug/product knowledge
*
c) ICH/GCP and local applicable regulation knowledge
*
d) Respect of confidentiality of subject information
Please rate your satisfaction with the site visits performed by the Teva Research Team.
Very Dissatisfied
Not Satisfied
Neutral
Satisfied
Very Satisfied
N/A
*
a) Planning of monitoring visits ahead of time
*
b) Showing up at site according to planned schedule
*
c) Providing a list of what needs to be accomplished during monitoring visits
*
d) Thoroughness of source data verification
*
e) Assisting with the audit/inspection preparation
*
Compared to other Sponsors' Clinical Research Teams with whom you are collaborating, would you say that the Teva Research Team is...
Much better
Somewhat better
About the same
Somewhat worse
Much worse
Don't know or never been involved with another Sponsor's Clinical Research Team
*
Overall, how satisfied are you with Teva's new Web-based Electronic Data Capture System (Oracle RDC)?
Very Dissatisfied
Not Satisfied
Neutral
Satisfied
Very Satisfied
Not Applicable
*
If you could specify ONE thing that the Teva Research Team does best, what would it be?
*
If you would have ONE thing you would recommend the Teva Research Team to improve on, what would it be?
Are there any additional comments you would like to make?
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