JOB OVERVIEW

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. In this role, you will oversee the management of clinical trials, ensuring compliance with regulatory standards and Good Clinical Practice (GCP). You will be responsible for coordinating all aspects of clinical research studies, including patient monitoring, data collection, and documentation review. The ideal candidate will possess strong analytical skills and a solid understanding of medical terminology, FDA regulations, and clinical development processes.

EXPERIENCE

• Proven experience in clinical research coordination or a related field is essential.
• Supervising experience within a clinical setting is highly desirable.
• Familiarity with clinical trials management processes and documentation practices.
• Strong knowledge of medical terminology, FDA regulations, and Good Clinical Practice (GCP).
• Experience with EMR systems for efficient data management is preferred.
• Background in nursing or clinical laboratory experience is advantageous.
• Proficiency in phlebotomy techniques and blood sampling procedures is a plus.
• Excellent analysis skills with the ability to interpret complex data sets effectively. Join our team as a Clinical Research Coordinator where you can contribute to advancing medical knowledge while ensuring the highest standards of patient care and compliance in clinical research settings.
• Preferred CCRC
  Job Type: Full-time
  Pay: $24.00 - $37.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Ability to Commute:

• Prescott Valley, AZ 86314 (Required)

Ability to Relocate:

• Prescott Valley, AZ 86314: Relocate before starting work (Required)

Work Location: In perso

• Supervise clinical trial activities and coordinate study logistics to ensure adherence to protocols.
• Manage patient recruitment, screening, and monitoring throughout the clinical trial process.
• Conduct thorough documentation reviews to ensure accuracy and compliance with regulatory requirements.
• Collect and manage data in accordance with CDISC standards and Good Clinical Practice guidelines.
• Utilize statistical software for data analysis and reporting findings as required.
• Maintain compliance with HIPAA regulations while handling sensitive patient information.
• Collaborate with clinical laboratory teams to facilitate blood sampling and vital signs monitoring.
• Ensure proper training and support for staff involved in clinical trials management.
• Act as a liaison between sponsors, regulatory bodies, and study participants to facilitate smooth operations.