- Den Haag, Nederland
- 22 oktober 2025
Opleiding
Ervaring
Efficiently and accurately perform data collection/reporting/quality assurance/regulatory compliance for complex data and sample intensive Phase I, II, & III sponsored Pediatric Neuro-Onc clinical trials
Schedule patient assessments/data collection for 50+ patients within protocol windows
Comply with all FDA regulations/CFR/ICH/GCP/MSK SOP/IRB protocols/Report SAEs/external safety events
Maintain investigator site files at MSK/participate in site initiation and interim monitor visits
Confirm training is recorded from site initiation of a protocol/amendments/addition of new investigators
Ensure quality and integrity of data/resolve sponsor queries/troubleshoot/solve problems/self-audit