Certified Clinical Research Coordinator

• Highly motivated and detail-oriented Clinical Research Coordinator with more than five years of experience in clinical trials and research operations.
• Skilled in coordinating and managing multiple clinical study protocols simultaneously, with experience overseeing more than four active protocols at one time.
• Bilingual professional with strong communication, multitasking, and interpersonal skills, capable of effectively collaborating with investigators, participants, sponsors, and multidisciplinary research teams.
• Ensures all deviations, violations, AEs, and SAEs are captured, recorded, followed, and reported to Sponsor/IRB in a timely manner.
• Experienced in EDC data entry and maintaining accurate clinical trial documentation.
• Extensive knowledge of FDA regulations, ICH Good Clinical Practice (GCP) guidelines, HIPAA compliance, and clinical trial procedures.
• Proficient in participant recruitment, informed consent processes, patient monitoring, phlebotomy, data collection, EMR systems, and regulatory submissions.
• Consents study participants following the Site’s SOPs.
• Proven ability to maintain accurate study records, ensure protocol compliance, and support the successful execution of clinical trials while prioritizing participant safety and data integrity.
• Confirm with the Front desk personnel, Laboratory technicians, and Assistant CRC, subjects scheduled for the following day.
• *Education and

Experience

*

• Associate degree or its equivalent required, Bachelor’s degree on related field preferred.
• Foreign Medical Graduate, or Registered Medical Assistant preferred.
• 2+ years of Clinical Research experience preferred.
• *Skills*: MUST BE BILINGUAL
• *

Schedule

• Monday to Friday – 8:00 am – 4:30 pm, unless otherwise indicated.
• *Work Location*: In person

Pay: $23.00 - $35.00 per hour Work Location: In person