Clinical Research Coordinator 3 - Multiple Myeloma
University of Miami · Miami, FL · 2 days ago
AnalystFull-time
Core Job Summary
The Clinical Research Coordinator 3 serves as an experienced clinical research professional responsible for planning, implementing, monitoring, and evaluating multiple clinical research protocols. This role manages multiple studies' daily operations, coordinates study recruitment, ensures study integrity, and mentors less experienced Clinical Research Coordinators.
Core Responsibilities
- Coordinates the implementation of multiple complex clinical research protocols.
- Develops SOPs and templates with guidance from the PI/Clinical Research Manager.
- Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.
- Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations.
- Plans and operationalizes strategies to monitor, document, report, and follow-up on unanticipated occurrences and protocol deviations.
- Develops and implements preventive/corrective actions.
- Develops, disseminates, and assures adherence to study-related clinical research best practices/scientific manuals.
- Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.
- Provides leadership in identifying and working through ethical conflicts arising during protocol implementation and refers these conflicts to the Research Ethics Team for consults as needed.
- Organizes/manages site visits and internal/external auditing activities as assigned.
- Captures and coordinates research team meetings; assures communications across-the-board.
- Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
Core Qualifications
- Education: Bachelor’s degree in relevant field required.
- Certification and Licensing: Current Research Coordinator certification by the Association of Clinical Research Professionals or Society of Clinical Research Associates for a minimum of 6 months.
- Experience: Minimum 4 years of relevant experience required.
- Knowledge, Skills and Abilities: Learning Agility, Teamwork, Technical Proficiency, Communication.