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INVESTIGATORS

SCR has a continuous need for qualified investigators and research sites to assist with clinical research trials. If you are an interested, experienced investigator, you may fill out and submit the automated investigator background information (IBI) form below, which will allow us to enter your information into our investigator database.

This database is used as a primary source for recruiting appropriate investigators for clinical trials we conduct on behalf of our sponsors. Information such as your medical specialty and subspecialty, phase

preference and diseases of interest, is critical to SCR when we are in the process of recruiting investigators for new and ongoing clinical trials. Further, it helps ensure you are only contacted for trials in which you have an interest. If you prefer not to submit an online IBI form, you may manually send in a copy of investigator background information form. You may also update your information already in our investigator database by simply contacting us.

INVESTIGATOR BACKGROUND INFORMATION FORM

Please read the following authorization agreement

Investigator Data Protection Authorization

SCR is committed to respecting the privacy of its clinical research investigators.  We recognize that when you choose to provide us with information about yourself, you trust SCR to act in a responsible manner.  SCR has enacted internal procedures, that are reviewed and monitored from time to time to ensure that your information is used responsibly and in accordance with applicable law.   These procedures require that the processing of personal data, both automated and manual, meet with the following data protection principles:

• be processed fairly and lawfully

• be obtained only for specified and lawful purposes, and not be processed in any incompatible manner

• be adequate, relevant and not excessive

• be accurate and, where necessary, kept up-to-date

• not be kept for longer than is necessary

• be processed in accordance with the rights of data subjects

• be protected by appropriate security measures

• not be transferred to third parties unless adequate level of data protection exist.

Data Processing

All processing of personal data is, by consent, for the purposes listed above and under the control of the data controller.  Individuals have the right to:

• copies of their data

• correct their data

• prevent processing for direct marketing

• withdraw consent to processing with its consequential effects

• prevent non-core purpose disclosures and

• prevent trans-border disclosures to third parties where there are inadequate data protection arrangements.

Trans-border data flows

SCR may transfer personal data to third parties as required for the conduct of clinical studies.  Personal data will only be transferred to third parties following receipt of assurance that the recipient will provide adequate data protection arrangements.

Data Controller

All communications, queries and subject access requests that are related to data protection issues should be e-mailed to info@globalspectrumcr.com for action or response on behalf of SCR.

By clicking on "ACCEPT" below, I agree that the following information about myself may be retained by SCR in the global investigator database and individual study files, as required.

• investigator name and contact information

• office/practice location, type, amenities and research staff

• medical specialty and patient population information

• affiliation with a site management organization (SMO) and SMO information

• historical and current information regarding participation in SCR projects

• other relevant information to allow selection for appropriate clinical trials in the future

• select financial information to allow for reimbursement of investigator grants

I understand that the above data will be used for the purpose of conducting clinical trials and may be transferred to the clinical trial sponsor, FDA or other regulatory bodies.

I hereby consent to SCR (the "Data Controller") the use, processing and transmission of information relating to me obtained by SCR.

I accept and agree to the investigator data protection Authorization (given above).