Clinical Research Coordinator

Job Summary
The Clinical Research Coordinator plays a pivotal role in the management and execution of clinical trials. This position involves overseeing the day-to-day operations of clinical studies, ensuring compliance with regulatory requirements, and maintaining high standards of patient care. The ideal candidate will have a strong background in clinical research, excellent organizational skills, and a commitment to upholding Good Clinical Practice (GCP) guidelines.

Duties

• Coordinate and manage all aspects of clinical trials from initiation to completion.
• Conduct thorough documentation reviews to ensure accuracy and compliance with study protocols.
• Monitor patient progress throughout the study, ensuring their safety and well-being.
• Maintain knowledge of medical terminology and clinical development processes.
• Implement compliance management strategies to adhere to regulatory standards.
• Assist in blood sampling procedures as needed for study assessments.
• Collaborate with cross-functional teams to facilitate effective communication and project execution.
• Prepare and submit necessary reports to regulatory bodies as required.
• Provide training and support to staff involved in clinical trials management.

Requirements

• Proven experience in managing clinical trials from startup to closeout.
• Experience running clinical trials across multiple therapeutic areas.
• Excellent documentation review skills with attention to detail.
• Strong understanding of Good Clinical Practice (GCP) guidelines.
• Experience with compliance management within a clinical research setting.
• Background in nursing or relevant healthcare experience is preferred but not mandatory.
• Strong organizational skills with the ability to manage multiple tasks simultaneously.
• Effective communication skills, both verbal and written, for interactions with patients, staff, and regulatory agencies.

This role is essential for advancing medical research while ensuring the highest standards of patient care are maintained throughout the clinical trial process.

Job Type: Full-time

Pay: $24.00 - $28.00 per hour

Expected hours: 40 per week

Benefits:

• 401(k)
• 401(k) matching
• Flexible schedule
• Paid time off
• Professional development assistance
• Relocation assistance

Work Location: In person