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University of Miami · 12 hours ago

Clinical Research Coordinator

Miami, FL

Full-time

Onsite

Mid Level

4+ years exp

The University of Miami is a leading academic medical center providing innovative patient care and education. They are seeking a Clinical Research Coordinator 3 to lead and manage multiple clinical research protocols, ensuring compliance with regulatory standards and participant safety while mentoring junior coordinators.

Higher Education

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

Coordinates research team meetings; assures communications across-the-board

Assures synchronization of study visits/procedures/ clinical tests with data collection schedules, established time-points; manages progress of study participants through protocol; expedites overall study progression

Coordinates the compilation of information needed for research reports; peer-reviewed publications; develops strategies to disseminate information to clinical personnel, professional audiences and stakeholders

Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies

Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies

Adheres to University and unit-level policies and procedures and safeguards University assets

Qualification

Clinical research protocolsStudy coordinationRegulatory complianceSOP developmentSample processingLearning agilityTechnical proficiencyTeamworkCommunication