Clinical Trials Coordinator

2 weeks ago


Torrance, California, United States The Lundquist Institute Full time
Position Overview:

The Lundquist Institute is seeking a dedicated professional to assist in the management of clinical research studies. This part-time role involves various responsibilities aimed at ensuring the smooth operation of clinical trials.

Essential Qualifications:

  • A Bachelor's Degree is preferred, particularly for those interested in a medical career.
  • Bilingual proficiency in English and Spanish is required.

Key Responsibilities:

  • Oversee the management of clinical trials, including patient interactions and document handling.
  • Ensure compliance with clinical trial protocols while managing participant involvement.
  • Facilitate communication, planning, and scheduling of necessary meetings and appointments.
  • Coordinate and supervise clinical research projects from initiation to completion.
  • Maintain adherence to all relevant regulations and guidelines.
  • Manage study-related documentation, including informed consent forms and research protocols.
  • Accurately collect and record data in a timely manner.
  • Perform phlebotomy as required (training will be provided upon hiring).
  • Review and confirm the accuracy and completeness of documentation.
  • Monitor participant progress throughout the study duration.
  • Uphold high standards of quality control and data integrity.
  • Follow Good Clinical Practice (GCP) guidelines diligently.

Compensation:
$24 per hour.

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