JOB SUMMARY

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to oversee and manage clinical trials from initiation through completion. The ideal candidate will possess strong supervisory experience and a solid understanding of clinical research processes, ensuring compliance with FDA regulations and Good Clinical Practice (GCP). This role involves working closely with patients, healthcare professionals, and research teams to facilitate the successful execution of clinical studies.

REQUIREMENTS

• Bachelor’s degree in a relevant field such as nursing or life sciences; advanced degree preferred.
• Proven experience in clinical trials management with a strong understanding of FDA regulations and GCP guidelines.
• Familiarity with EMR systems for efficient data management and patient record keeping.
• Strong analytical skills with experience in data collection and analysis within a clinical research setting.
• Excellent communication skills to effectively interact with patients, healthcare professionals, and research teams.
• Previous experience in supervising staff or coordinating teams is highly desirable.
• Knowledge of clinical laboratory practices is a plus, along with familiarity with patient monitoring techniques. Join our team as a Clinical Research Coordinator where you will play a vital role in advancing medical research while ensuring the highest standards of patient care and compliance are met throughout the clinical trial process.
  Job Type: Part-time
  Pay: $25.00 - $30.00 per hour
  Expected hours: 25 per week

Benefits:

• Flexible schedule

Work Location: In perso

• Supervise and coordinate the daily operations of clinical trials, ensuring adherence to study protocols and timelines.
• Manage patient recruitment, monitoring, and retention throughout the study duration.
• Review documentation for accuracy and completeness, ensuring compliance with regulatory requirements.
• Collect and manage data from clinical trials, utilizing statistical software for analysis.
• Conduct patient assessments, including vital signs monitoring, blood sampling, and phlebotomy as required.
• Collaborate with clinical laboratory personnel to ensure proper handling of specimens.
• Maintain knowledge of medical terminology and clinical development processes to effectively communicate with stakeholders.
• Ensure compliance with HIPAA regulations in all patient interactions and data management activities.
• Prepare reports on study progress, findings, and compliance for internal review and regulatory submissions.
• Provide training and support to research staff on CDISC standards and documentation practices.