Clinical Research Coordinator

2 weeks ago


Covina, United States SQRL Full time

This role will be onsite in Covina, CA

Responsibilities:

  1. Study Coordination:
  • Coordinate and oversee the planning and execution of clinical research studies per protocols and regulatory requirements.
  • Work closely with principal investigators and other study team members to ensure the successful implementation of research projects.

  1. Regulatory Compliance:
  • Ensure adherence to regulatory standards and guidelines, including but not limited to FDA regulations, ICH/GCP guidelines, and institutional policies.
  • Prepare and submit regulatory documents for study approval and maintain accurate and up-to-date regulatory files.

  1. Participant Recruitment and Informed Consent:
  • Recruit and screen eligible participants for clinical trials.
  • Obtain informed consent from study participants and maintain proper documentation.

  1. Data Collection and Management:
  • Collect, record, and manage study data accurately and efficiently.
  • Implement data quality control procedures and ensure data integrity throughout the study.

  1. Communication and Collaboration:
  • Serve as the primary point of contact for study participants and liaise with interdisciplinary team members, including physicians, nurses, and laboratory personnel.
  • Communicate regularly with sponsors, monitors, and regulatory authorities as needed.

  1. Training and Development:
  • Provide training to research staff and ensure ongoing education on study protocols, procedures, and regulatory requirements.

Qualifications:

  • Must have prior experience as a Clinical Research Coordinator in a healthcare or research setting (3+ years)
  • Must be Bilingual; Spanish
  • Must be certified in phlebotomy


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