Monitorforhire Mobile vs myTI

What if CRAs didn’t have to search for trials? With a database of 1,000 sponsors and more than 5,000 monitors spanning more than 60 countries, the jobs will finally search for you! MonitorForHire.com is a patented, web-enabled management tool for locating and contracting available, independent clinical research monitors for clinical trials. This on-the-go tool enables monitors to keep track of their current projects, view open project invitations, log time, submit availability, and stay in touch with all of MonitorForHire.com’s opportunities. Who uses this app? Independent clinical research monitors in the following fields: • Pharmaceutical • Biotech • Medical Device • Contract Research Organization (CRO) Industry • Academic Institutions *Note: You must be a registered and approved monitor at MonitorForHire.com to use this app. Visit our webpage to sign up today. Features • Accept or reject open project invitations • Manage current projects • Submit availability (up to 11 months forward) • Report time for current projects • Receive push notifications for pending project invitations, as well as for active projects

The myTI application is a mobile extension of Trial Interactive, a TransPerfect Life Sciences cloud based e-clinical platform. Trial Interactive was designed by clinical professionals for clinical professionals to meet the end-to-end needs of the clinical trial lifecycle. For the first iteration, myTI enhances the Trial Interactive eTMF module, placing key eTMF processes at the fingertips of study teams at all times. Document capture, query and resolution is essential to a trial’s success and for the health of the eTMF. Building on the Trial Interactive mission to streamline and simplify global product development, myTI reduces the need to transport large quantities of paper for scanning and expedites the upload of documents. Users login with their biometric login and safely capture documents with their device camera without storing images on the device itself. Captured images are easily uploaded and coded directly to the eTMF. myTI provides constant access to document query and site statuses so users can proactively manage study documentation and data. Users can experience key advantages of eTMF anytime, anywhere they need it. The mobile experience provides role-specific access for all study professionals (CRAs, project managers, TMF leads, etc.). Highlights of myTI include: - Document Submission: Securely capture documents with the mobile device camera and add to the eTMF - Query Resolution: Review documents with queries and resolve them right from the mobile interface - Document Status: view status, metadata, and update/re-submit expired documents from your phone or tablet - Cloud-Based: Built on a secure cloud service, myTI sends the images of documents directly into the eTMF - iPhone Versions 10.3+ with support back to model 5S - Biometric login: Secure and configurable for devices that support Touch ID® and Face ID® - Document Detection: Similar to check depositing in banking applications, just hold your mobile device over the document and myTI captures the image immediately, ensuring the image meets quality standards - Perspective Correction: myTI straightens and adjusts scanned documents prior to converting them into PDF files and uploading into the eTMF - 21 CFR Part 11 Compliant: Complies with regulatory standards for hosting eTMF documents About TransPerfect Trial Interactive TransPerfect’s Trial Interactive solution provides a collaborative web-based platform for study start-up and eTMF that enables sponsors, CROs, IRBs, central laboratories, and other vendors to maintain and update clinical trial documentation in a secure online environment. With fully searchable solutions including investigator portals, Trial Interactive streamlines study timelines and reduces the administrative burdens of global clinical trials. As part of TransPerfect’s Life Sciences division, Trial Interactive is dedicated to working with clients on a global, collaborative level, supporting a wide range of requirements including e-feasibility, eTMF review/reconciliation, pharmacovigilance and safety management, endpoint adjudication, and product licensing and alliance management.