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  1. Surveys
  2. 2010
  3. June
  4. F
  5. Final Reminder testing-Site Satisfaction Survey 20
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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?
 
 
* Please indicate your country:
 
 
 
* 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 (eg. completion of CRFs, dispensing of Investigational Medicinal Product, handling laboratory specimen, etc.)
* 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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