Clinical Trial Data Collection Expert

Our upcoming clinical trial is moving into the data-collection phase, and I need a medical researcher who has hands-on experience capturing trial data accurately and in compliance with GCP. You will take the lead on setting up and managing the day-to-day flow of information from study sites into our electronic data-capture platform (REDCap or a similar EDC), making sure every case report form is complete, consistent, and audit-ready. Key tasks you will handle include: • Configuring or refining eCRFs and validation rules in the EDC. • Training site coordinators on correct data-entry procedures and protocol adherence. • Performing real-time data checks, generating queries, and resolving discrepancies with the sites. • Producing clean, well-annotated datasets ready for the biostatistics team. Deliverables are accepted when: • All enrolled-patient records pass internal edit-check logic with <2 % outstanding queries. • A final, locked database and accompanying data-handling report are supplied in both CSV and SAS-ready formats. Daily collaboration happens over Slack and Zoom, with weekly progress snapshots stored in our Git-tracked documentation repo. If you have previous experience with phase II oncology trials, Medidata Rave, or CDISC standards, highlight that in your proposal—it will speed up onboarding. Timeline: first site opens in three weeks, so setup needs to be finalised within ten days of project start, followed by ongoing data-cleaning support through database lock.