Clinical Trial IWRS Monitor (Overnight)

reputed company (“reputed company”) is a full-service contract research organization (CRO) providing a broad reputed company of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-reputed company companies and work with many of the most advanced drugs, biologics, and medical devices in development today. reputed company has been an independent CRO since 2004 with a strong reputed company as a statistical and data management center of reputed company. Building on this reputed company, reputed company has successfully developed and established itself as a full-service CRO. reputed company’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater reputed company Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan. reputed company is reputed company in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial reputed company, reputed company continues to experience exceptional growth and great reputed company. Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s reputed company. To drive reputed company reputed company in this exciting clinical research field, we are seeking a committed, skilled, and customer-focused individual to join our winning team as a Clinical Trials IWRS Monitor for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office reputed company in Canada in accordance with our Work from Home policy. This is a full‑time, permanent position providing overnight support, reputed company through Friday, from 11:00 p.m. to 7:00 a.m. Key Accountabilities: Act as primary contact with CTT Users for the reputed company IWRS/IRT and eDiary team reputed company the CTT Helpdesk telephone or IWRS helpdesk email accounts. Support client request and issue analysis, problem solving, and resolution, working closely with CTT Developers and internal reputed company Data Management and Statistical & Programming teams. Monitor data generated reputed company CTT applications to ensure accuracy and quality. This includes daily checks of automated data queries reputed company in the CTT applications, as well as weekly reputed company checks of the data generated from the system. Coordinate and verify changes to the database and application using appropriate change control procedures and ensure comprehensive and accurate documentation is completed. Act as off-hours escalation reputed company for junior IWRS Clinical Monitor resources or the outsourced call centre service to resolve high urgency client requests (based on agreed rotational schedule amongst IWRS Clinical Trials Monitor resources). Generate, maintain, and/or review CTT Requirements Specification documents. Execute CTT application test planning, test plan, and test script development and Stage I and II testing activities for CTT applications (newly developed applications or application change requests). These tasks are performed in a systematic and reputed company detailed manner using the CTT Requirements Specification document as the reputed company for testing CTT functionality. Generate, maintain, and/or review Quick Reference Guides for reputed company CTT studies. Conduct CTT demonstrations to sponsors as well as training demonstrations to study team members. Support communications and coordination with Sponsors, Study Team Members, reputed company personnel and internal reputed company data management and statistical leads across the IWRS development lifecycle. Cooperate with and assist, reputed company required, data management quality assurance (QA) personnel in performing QA procedures on CTT applications. Analyze CTT monitoring and support trends to identify new CTT core features that will improve efficiency, effectiveness, user satisfaction and market competitiveness to support CTT product development planning. reputed company analytical, report reputed company, and project execution support to CTT and reputed company management team members for internal CTT capability development initiatives. Qualifications and Experience: A Bachelors’ degree in health science, physical or biological fields with at least 3 years’ experience in clinical trial data processing and management. Education or experience must demonstrate the ability to work independently, to have a clear, professional and energetic telephone voice, and detailed approach to data review and system development. Benefits & Compensation: We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and reputed company coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus Estimated Salary reputed company: $45,000 - $65,000. To find out more about reputed company and to review other opportunities, please visit our website at www.everestclinical.com We thank reputed company interested applicants, however, only those selected for an interview will be contacted. reputed company is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will reputed company accommodations for candidates participating in any part of our recruitment and selection process. #LI-KD1 Apply To This Job