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  • Privacy Policy

    Medical Research Network Limited and its group companies (the MRN, the Company, VCTC, we, us) are committed to protecting and respecting the privacy of clinical trial participants, health care professionals, customers, website visitors and job applicants, and this includes their personal and health related information.

    This policy and any other documents referred to within it, sets out the basis on which any personal data (or personal information) we collect or that is provided to us, will be processed by us.

    Any questions about how we process personal data, or if you would like to exercise your data subject rights, please email us at dataprivacycommittee@themrn.co.uk.

    As an organisation, the MRN have a responsibility to safeguard all personal data that it holds. The Company is responsible for ensuring compliance with applicable international and local data protection laws and regulations, including but not limited to the Data Protection Act 2018 (DPA 2018), the United Kingdom General Data Protection Regulations (UK GDPR), Regulation (EU) 2016/679 (the General Data Protection Regulation) (GDPR), the Act on the Protection of Personal Information (APPI), the Health and Insurance Portability and Accountability Act (HIPAA) and, the privacy and confidentiality requirements of Good Clinical Practice (GCP).

    The MRN has a number of internal policies, procedures and processes for safeguarding personal information, and these conform to applicable data protection principles. To ensure personal data receives an adequate level of protection when transferred between the various parts of the MRN’s organisation, the MRN has put in place an Intra Group Data Sharing Agreement and where applicable Standard Contractual Clauses, these together with additional supplementary measures, ensure personal data is treated by all of its offices in a way which is consistent with and respects the EU and UK laws on data protection.

    1. The MRN acts as a Data Controller for the following types of Personal Data:

    Job Applicant Data

    In this context, the MRN acts as Data Controller as it retains control over the purposes for processing personal data about its job applicants and the manner in which it does this.
    The types of personal data requested and ways it is processed are determined by the requirements of the country in which the position is located. Personal data collected directly from you when you apply for a role include name, address, contact information, work and educational history, references, identification documents. We may also collect personal data about you from third parties, such as your references, our employees who interviewed you, publicly available information and employment background checks.

    We collect and use your personal data for legitimate human resources and business management reasons including identifying and evaluating candidates for potential employment, as well as for future roles that may become available; record keeping in relation to recruitment; ensuring compliance with legal requirements, including diversity and inclusion requirements and practices; conducting background and criminal history checks as permitted by applicable law.

    If we wish to retain your personal data to consider you for future employment, we will seek your consent to do so.

    Your personal data may be accessed by recruiters and interviewers in the country where the position for which you are applying is based, as well as by recruiters and interviewers working in different countries within our organisation. Individuals performing administrative functions and IT personnel may also have limited access to your personal data.

    If you accept an offer of employment, any relevant personal data collected during your pre-employment period will become part of your employment records.

    Customer Data

    In this context, the MRN acts as a Data Controller as we hold a database of individual business contacts. We may send you MRN-related marketing communications, as permitted by law. You will have the opportunity to opt in or out of our marketing communications and to change your mind at any time by clicking on the unsubscribe button at the foot of any marketing emails from us.

    For individuals sharing personal information with us in order to enquire about our services, we will use such personal information in order to provide the requested information and/or services.

    Website Visitors

    The MRN collects name and contact information from visitors to the MRN website who ask for further information regarding MRN’s services. The MRN uses this contact information to deliver the requested information to these visitors. The MRN also uses IP addresses for tracking virtual identities; for visitors with requests for information, this tracking is linked to real-world personal information.

    Third Party Websites.

    Our website contains links to third party websites. Links to those websites are not under our control. This policy does not apply to such websites. It is recommended that visitors review the privacy policy of each such website.

    When using our website, we may use “cookies” and/or tools to store and sometimes track information about you. For more details about cookies, please see our cookie policy.

    2. The MRN Acts As A Data Processor Or Sub-Processor For The Following Types Of Personal Data:

    Trial Participant Data

    The MRN acts as a Data Processor OR Sub-Processor of clinical trial data. The MRN processes personal information that is needed in order to perform clinical trial related services, such as in-home protocol visits for trial participants. The MRN uses personal information to conduct clinical trial related services and to manage the logistics relating to those services. The MRN takes responsibility for how it processes the information internally and for the manner by which it provides information to any approved subcontractors it might utilize to actually perform the services.

    The personal data and purposes for which trial participants’ personal data will be used by study sites and Sponsors will be addressed in more detail in the study specific consent documentation. As such, trial participants should look to that documentation to understand how their personal data is processed.

    Depending on the processing activity, the relevant Data Controller may be the study site and/or the Sponsor. The study site is responsible for the medical care of the trial participants and the Sponsor is responsible for the medical research the study concerns.

    Third Party Study Personnel

    The MRN acts as both a Data Controller and a Data Processor where third parties supporting clinical trials are concerned. In order to perform our services and to conform to ICH-GCP, the MRN is obliged to confirm that individuals from any third parties are suitably qualified and competent to do so. As such, the MRN holds CV’s/resumes of health care professionals who perform clinical trial support services and forwards these on to sites and customers. Furthermore, we may also store contact details of healthcare professionals who support our services. Under ICH-GCP, the MRN are also required to store and archive information relating to our services so that the clinical trial can be recreated in the future.

    Information Collection

    We may collect information about you:

    4. Security Measures

    We endeavor to take all reasonable steps to protect your personal information. Risk assessment, including assessing risks to the rights and freedoms of data subjects is at the heart of our information security management system. We do not, however, have any control over what happens between your device and the boundary of our information infrastructure. You should be aware of the many information security risks that exist and take appropriate steps to safeguard your own information.

    5. Data Sharing, International Data Transfers And Data Security

    The MRN shares data with processors and sub-processors, as well as third parties where necessary and permitted to perform the tasks the MRN carries out. The MRN is a global organization and uses appropriate measures, including the Data Sharing Agreement to protect the data that it processes between its entities. Data is encrypted and protected wherever possible and only kept in an identifiable format for as long as necessary. The MRN maintains the confidentiality, integrity and availability of data, and has robust policies for retention, archiving, disaster recovery and data disclosure rules so that the data in its entire life cycle is protected, while in the MRN’s care.

    MRN complies with the EU-US Data Privacy Framework (“EU-US DPF”), the UK Extension to the EU-US DPF and the Swiss-US Data Privacy Framework as set forth by the US Department of Commerce. For information on our certification to these Frameworks please see our Data Privacy Framework Policy.

    6. Clinical Trial Support Services

    The MRN provides a service to the clinical research community including a healthcare service, both services are regulated and bound by professional standards.

    Informing Trial Participants Of Access To And Collection Of Personal Data

    All trial participants are made aware of what happens to the personal data collected about them during a trial and who has access to it. Reference to the release of their information to third parties should be set out in the study specific consent documentation signed by or on behalf of individual trial participants.

    By referring a trial participant to the MRN, the site is confirming that the participant has consented to the trial and for their personal data being shared with the MRN and other third parties. The personal data collected is the minimum required in order for the MRN to provide the services.
    Health care professionals receive regular training by the MRN on their responsibilities for the handling and management of personal data.

    Access To Trial Participant Data
    Within the MRN, access to personal data is limited to only those personnel who are assigned to a specific trial within the MRN.
    All documents used as part of the MRN’s service that do not require directly identifying personal data use a unique identifier (number) instead of the participant’s name.

    7. Data Subject Access Rights

    A data subject whose personal information we hold, has certain rights. To exercise any of these rights, please email dataprivacycommittee@themrn.co.uk or use the information supplied in the ‘Contact us’ section below. To process a request, we will require the provision two valid forms of identification for verification purposes. Rights are as follows:

    8. EU Representation

    If you are based in the EU, and you wish to exercise your rights under the EU GDPR, or have any queries in relation to your rights or general privacy matters, please email our representative at dataprivacycommittee@themrn.co.uk.

    9. Contacting Us

    Any comments, questions or suggestions about this privacy notice or our handling of your personal data should be emailed to dataprivacycommittee@themrn.co.uk.

    Alternatively, you can contact us at:
    Data Privacy Committee
    Medical Research Network Limited
    Talon House
    Presley Way
    Crownhill
    Milton Keynes
    MK8 0ES

    10. Complaints

    Should you wish to discuss a compliant, please feel free to contact us using the details provided above. All complaints will be treated in a confidential manner.

    Should you feel unsatisfied with our handing of your data, or about any complaint that you have made about our handing of your data, you may have rights to file a complaint with a regulator in your jurisdiction. For the UK, this is the Information Commissioner’s Office, which is also our lead supervisory authority. Its contact information can be found at https://ico.org.uk/global/contact-us/.