Clinical Research Associate — Hematology · REMOTE

About the role

You carry a portfolio of hematology trial sites from qualification to close-out, and you own what happens s is a working monitoring role, not an oversight layer: you sit with the source documents, you know the coordinators by name, and when something at a site is about to become a problem, you are the person who saw it a month early.

• Conduct the full visit lifecycle — qualification, initiation, interim monitoring, and close-out — and manage your sites between visits
• Verify entered data against source records for accuracy, completeness, and patient safety, raising and resolving queries in the EDC
• Review informed consent documentation and subject safety information at every pass
• Surface protocol deviations early, document them plainly, and see corrective action through
• Assess and train site staff on protocol adherence where the site needs it
• Maintain investigational product oversight end to end: receipt, storage conditions, accountability, and return or destruction
• Keep site documentation flowing into the Trial Master File as the study runs, not after it ends
• Mentor newer CRAs — including accompanied visits for assessment and training — as the team grows

• Two or more years of monitoring experience as a Clinical Research Associate
• Hands‑on experience in hematologic malignancies; broader oncology depth strengthens a candidacy
• A four-year degree, or RN/BSN
• Written and spoken English at the standard your visit reports will be judged by
• Organized, exact, and effective without supervision — your sites are yours
• Fluent across CTMS, EDC platforms, and Microsoft Office
• Approximately 35% travel

• $46–$50 per hour.
• Medical, dental, and vision coverage;
• 401(k) with employer matching;
• Paid time off and holidays.