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Clinical Trials Coordinator

2 months ago


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

This part-time role involves supporting clinical research initiatives at The Lundquist Institute. The ideal candidate will have a strong foundation in medical sciences and a passion for advancing healthcare through research.

Essential Qualifications:

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

Key Responsibilities:

  • Oversee the management of clinical trials, ensuring effective communication with participants.
  • Ensure adherence to clinical trial protocols and regulatory compliance.
  • Plan and coordinate meetings and appointments related to research activities.
  • Manage the entire lifecycle of clinical research studies, from initiation to completion.
  • Maintain compliance with all relevant regulations and guidelines.
  • Handle study documentation, including informed consent and protocol management.
  • Accurately collect and record data in a timely manner.
  • Perform phlebotomy tasks as required (training will be provided upon hiring).
  • Review documentation for accuracy and completeness.
  • Monitor participant progress throughout the study duration.
  • Uphold high standards of quality control and data integrity.
  • Adhere to Good Clinical Practice (GCP) standards.

Compensation:
$24 per hour.