Research Coordinator

Requirements

• Adheres to patient care standards
• Communicates effectively
• Assists with screening patients, scheduling, and overseeing on-study requirements
• Attends study teleconferences with sponsors and clinical research organizations
• Provides protocol-specific education to clinical staff
• Facilitates meetings/teleconferences with sponsors, monitors, and auditors
• Reports serious adverse events, unanticipated problems, deviations, violations, and noncompliance
• Contributes to corrective and preventive action plans
• Identifies and intervenes to address barriers to informed consent
• Ensures informed consent is obtained prior to study-specific tasks
• Collaborates with the investigator to ascertain study patient eligibility
• Educates patients and families regarding protocol participation
• Provides patient education regarding required study procedures
• Coordinates, schedules, and ensures timely completion of protocol-required events
• Assesses patient's adherence to and documentation of self-administered protocol agents
• Collaborates with the investigator to determine disease response
• Ensures communication between research and clinical staff related to patient-specific care needs
• Maintains specified study documents
• Participates in the development of approved source documents
• Adheres to data management plan
• Ensures data integrity
• Enters data into electronic data capture
• Assists in troubleshooting data entry issues
• Ensures that relevant data from source documents are abstracted and entered into CRFs
• Maintains the privacy and confidentiality of patients' source documents

Benefits

• Paid Time Off
• 401k Matching
• Health and Welfare benefits
• Other forms of compensation