Senior Clinical Research Coordinator (Full time)
As a Senior Clinical Research Coordinator, you’ll be instrumental in managing complex oncology trials from initiation to close-out. We’re looking for a detail-oriented leader who can drive efficiency and ensure top-tier data integrity in Dallas/Ft Worth.
Qualifications:
- Expert Data Management & Reporting: Oversee data collection, entry into EDC systems, and comprehensive reporting of adverse events, maintaining high-quality data for all assigned trials.
- Proactive Patient Recruitment & Screening: Lead patient screening efforts within EMRs, manage updated screening logs, and communicate directly with investigators to identify eligible candidates for active trials.
- Master Patient Coordination & Consent: Facilitate all aspects of patient engagement, from obtaining informed consents (treatment, tissue/specimen) to educating patients on trial requirements and coordinating all research visits.
- Drive Study Execution & Compliance: Coordinate and track all patient activities throughout their trial participation, ensuring compliance with protocol requirements and meticulous documentation of deviations.
- Streamline Operational Processes: Develop and implement efficient logistical processes for patient onboarding and create internal QA procedures to ensure data accuracy and smooth monitoring visits.
- Cross-Functional Team Collaboration: Partner seamlessly with clinic staff for scheduling and visit needs, and provide essential training on protocol requirements to optimize team performance.
- Maintain Comprehensive Documentation: Organize and manage all paper and electronic source documentation, ensuring readiness for internal and external audits.
- Investigational Product Management: Prepare and maintain precise temperature and accountability logs for investigational products.
- Support Principal Investigator Oversight: Provide accurate patient status updates and comprehensive tracking data to assist PIs during recurring investigator and sponsor meetings.