Clinical Research Coordinator II at University of South Florida responsible for coordinating clinical research activities and ensuring participant data quality. Serving as main contact for sponsors and patients for specific research protocols.
About the role
- Clinical Research Coordinator managing administrative activities and compliance for clinical trials in the School of Medicine at Emory University. Guiding staff and interfacing with research participants.
Responsibilities
- Manages research project databases, develops flow sheets and other study related documents, and completes source documents/case report forms
- Provides guidance to less experienced staff
- Interfaces with research participants, determines eligibility and consents study participants according to protocol
- Approves orders for supplies and equipment maintenance
- Assists in developing recruitment strategies and conducting screenings for study participants including interviews and questionnaires
- Supervises collection of study specimens and processing
- Establishes case packages for study procedures, monitors scheduling of procedures and charges, coordinates other services as needed
- Ensures compliance with research protocols, reviews case report forms and audits for accuracy with source documents, attends monitoring meetings with sponsors
- Prepares regulatory submissions
- With appropriate credentialing and training may perform phlebotomy or diagnostics.
- Performs related approved responsibilities as required.
Requirements
- High School Diploma or GED and five years of clinical research experience
- Two years of college in a scientific, health related, or business administration program and three years clinical research experience
- Licensed as a practical nurse (LPN) and two years clinical research experience
- Bachelor's degree in a scientific, health related, or business administration related program and one year of clinical research experience
- Master's degree, MD or PhD in a scientific, health related or business administration program.
Benefits
- Premium pay eligible per departmental guidelines
- On-call work required
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
Clinical Research Study Assistant supporting neurology clinical research at WashU. Assisting in data management, document compliance, and coordinating study personnel interactions.
Seeking an Advanced Practice Provider for part - time clinical research role at SRI. Flexible hours supporting studies in Plymouth, MI with potential for growth into longer - term positions.
B(
Clinical Research Coordinator II in Boston managing research studies and patient eligibility tracking. Collaborating with a research team for patient recruitment and data processing in healthcare.
RN Clinical Research Coordinator overseeing successful implementation of oncology clinical research studies at Florida Cancer Specialists. Collaborating with Principal Investigator and team for effective study management.
Clinical Research Study Assistant responsible for participant recruitment and data collection in Radiology at the Gordon Precision Neuroimaging Lab. Ensuring adherence to protocols and quality of information.
Clinical Research Coordinator providing assistance on clinical research studies including recruiting and organizing data. Supporting patient consent and clinical tests within a hybrid work setting.
Clinical Research Coordinator overseeing multi - site orthopedic clinical studies, providing comprehensive information and ensuring compliance with regulatory standards. Collaboration with researchers for study design and team training is key.
Expert responsible for cleaning strategies for reusable medical devices at Coloplast. Collaborate on innovative solutions for intimate healthcare needs in an international R&D team.
Clinical Research Coordinator facilitating clinical studies in food allergy research at Mass General Brigham. Recruiting subjects, collecting data, and ensuring regulatory compliance for trials.