Analgesia • CNS/Neuroscience • Rare Disease • Pediatrics • Oncology
1001 - 5000
💰 Venture Round on 2016-10
2 days ago
Analgesia • CNS/Neuroscience • Rare Disease • Pediatrics • Oncology
1001 - 5000
💰 Venture Round on 2016-10
• Delivering high-quality, timely monitoring reports for sponsor approval per Clinical Monitoring Plan timelines. • Scheduling site visits for monitoring as required by protocol monitoring visit windows. • Monitoring data — remotely, on site, and via other approved modes — with a focus on data integrity and patient safety, in accordance with specific country regulations. • Planning day-to-day activities for study monitoring and setting priorities by site. • Preparing for and conducting qualification, study initiation, interim monitoring, and close-out visits at investigator sites. • Providing accurate and timely trip reports and records of hours worked. • Managing query resolution with study sites and Premier Research data management operations.
• Undergraduate degree or its international equivalent in clinical, science or health related field from an accredited institution or a licensed healthcare professional. • Previous clinical research and independent site monitoring experience. • Working knowledge of local and international regulatory procedures, and monitoring activities
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