What are the responsibilities and job description for the Clinical Research Coordinator position at Optimal Research Sites?
Clinical Research Coordinator Duties: - Coordinate and oversee clinical research studies from start to finish - Ensure compliance with all applicable regulations and guidelines - Manage study documentation, including informed consent forms and study protocols - Collect and record data accurately and efficiently - Perform vital signs measurements and phlebotomy as needed - Review documentation for accuracy and completeness - Monitor patients throughout the duration of the study - Ensure adherence to Good Clinical Practice (GCP) standards Experience: - Previous experience in clinical research or a related field is preferred - Knowledge of clinical development processes and compliance management systems - Familiarity with clinical laboratory procedures and data collection methods - Proficient in vital signs measurements and documentation review - Ability to monitor patients effectively and ensure their safety during the study - Understanding of Good Clinical Practice (GCP) guidelines If you are a detail-oriented individual with a passion for clinical research, we want to hear from you. Apply now to join our team as a Clinical Research Coordinator. PLEASE ONLY APPY IF YOU HAVE EXPERIENCE AND ARE LOCAL OR WILLING TO COMMUTE.
Job Type: Full-time
Pay: $55, $62,000.00 per year
Benefits:
- 401(k)
- Paid time off
- Professional development assistance
License/Certification:
- GCP (Required)
Work Location: In person
Salary : $62,000