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Clinical Research Protocol Specialist
2 months ago
Position: Clinical Protocol Coordinator
Location: PriceSenz
Weekly Hours: Full-Time: 30-40 hours per week
Position Summary:
The Clinical Protocol Coordinator will play a pivotal role in supporting clinical and biospecimen research initiatives at PriceSenz. This position requires a detail-oriented and organized individual with excellent communication skills to facilitate the coordination of clinical research projects.
Key Responsibilities:
- Research Coordination: Assist in the management of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Data Management: Collect and analyze research data, ensuring accuracy and timely submission of necessary documentation.
- Protocol Development: Prepare and submit new IRB protocols, collaborating with research staff to ensure all regulatory forms are completed.
- Monitoring and Reporting: Track recruitment and enrollment status, prepare reports, and participate in monitoring activities.
- Quality Assurance: Assess study protocols for compliance with federal standards and generate quality assurance reports.
Qualifications:
Education: Bachelor’s degree in a relevant field.
Skills:
- Proficient in managing clinical trial materials and coordinating project meetings.
- Experience with biomedical research informatics systems.
- Strong understanding of regulatory compliance and Good Clinical Practices.
Additional Information:
The Clinical Protocol Coordinator will also be responsible for developing training materials for new research coordinators and ensuring adherence to best practices in clinical research.
