Clinical Research Coordinator - Loma Linda, CA

IQVIALoma Linda, CA
2d$35 - $42Onsite

About The Position

We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Requirements

  • High School Diploma or equivalent education and experience.
  • Minimum 1 year of relevant work experience in clinical research (preferred).
  • Working knowledge of clinical trials, GCP principles, and medical terminology.
  • Strong attention to detail and ability to establish effective working relationships.
  • Please note: This position is not eligible for sponsorship.

Responsibilities

  • Perform a variety of complex clinical procedures, including ECG, spirometry, sample collection, and vital signs.
  • Phlebotomy is required; pediatric experience is highly preferred.
  • Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
  • Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
  • Recruit, screen, and orient volunteers, ensuring their safety and well-being throughout the study.
  • Collect and accurately record clinical data in case report forms (CRFs).
  • Collaborate with investigators and monitors, addressing queries and ensuring data quality.
  • Act as a volunteer advocate and maintain a safe environment in accordance with Health and Safety policies.
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