appreciates the dedication and commitment that sites and their staff bring to clinical research studies. Our ability as a CRO to help pharmaceutical companies develop new drugs and medical devices would not be possible without your help.
If you are interested in working with PAREXEL on clinical research studies, please take a few minutes to answer the following questions.
Thank you very much for your time.
Global Site Solutions
If you have questions about this survey, please contact us via E-mail:
Data Protection Consent for Online Survey Participants
PAREXEL International Corporation and its affiliates (collectively, “PAREXEL”) appreciates the dedication and commitment that investigators and their staff bring to clinical trials or observational research studies. Our ability as a CRO to help pharmaceutical companies develop and test new drugs and medical devices would not be possible without your help.
For the purpose of assessing your eligibility for future clinical trials or observational research studies, PAREXEL would like to process information about you which is collected: (i) when you show your interest in participating in clinical trial or observational research studies by completing the Online Survey available on our website
; (ii) when you complete a feasibility or Pre-Qualification survey for a specific clinical trial or observational research study; and (iii) as part of the management of clinical trials or observational research studies where PAREXEL is acting as a CRO for Sponsors. This will include your name, surname, contact details and information about your patient pool, recruitment, enrolment, treatment practices, level of interest in the offered opportunity or generally in clinical trials or observational research studies, professional experience, participation and performance to past, present and future clinical studies and will consequently contain personal data about you.
As part of this assessment, PAREXEL may disclose your personal data to third parties including, affiliates, clients, contractors, vendors or service providers. The recipients of your personal data may be located outside the European Economic Area ("EEA"), including the United States, which may not have data protection laws equivalent to those in the EEA. In such a case, the necessary measures will be taken to ensure the safety of your personal data with applicable data protection laws.
You have a right to access your personal data and to request the correction of any error in relation to your personal data or to object to the processing of your personal data. You can exercise those rights by sending a request to PAREXEL International Corporation, 195 West Street, Waltham, MA, 02451, USA or at email@example.com.
By ticking the box below, you expressly consent to the processing of your personal data by PAREXEL for the purpose of assessing your eligibility to participate in future clinical trials and observational research studies. You can withdraw your consent to such processing by sending a written request at to PAREXEL International Corporation, 195 West Street, Waltham, MA, 02451, USA or at firstname.lastname@example.org However, you understand and acknowledge that the processing of your personal data for the purpose of assessing your eligibility for future clinical trial and observational research studies is different and completely separate from the processing of such personal data by PAREXEL for clinical trial or observational research study management purposes and therefore that such withdrawal will not in any way affect or limit PAREXEL's ability to continue to process your personal data for the purpose of clinical trial or observational research study management and to comply with requirements from sponsors and to meet regulatory and legal obligations.
The supply of my personal data and the personal data I provide on behalf of the site to PAREXEL is voluntary. I acknowledge that if I do not wish PAREXEL to collect, process or disclose such data in accordance with this statement, I will not attempt to provide PAREXEL with such data.
Please answer question Data Protection Statement before continuing.
Do you confirm that you are interested in Clinical Research and in cooperation with PAREXEL
and consent to the processing of your personal data as set forth above?
Yes, I agree
No, I am not interested
* Denotes a required response
© Copyright 2000-2017 PAREXEL International