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Research Coordination Specialist

2 weeks ago

Fremont, California, United States Medix™ Full time

About the Role:

We are seeking a highly skilled Clinical Research Coordinator to join our team at Medix™. As a key member of our team, you will be responsible for coordinating research patient visits and ensuring adherence to protocols, timelines, and regulatory requirements.

Your primary responsibilities will include recruiting, screening, and enrolling study participants, obtaining informed consent, and ensuring participants' rights and safety are upheld throughout the study. You will also be responsible for collecting, processing, and managing study data in compliance with Good Clinical Practice (GCP) guidelines.

A successful candidate will have a strong understanding of GCP guidelines, excellent communication skills, and the ability to manage multiple tasks simultaneously. Experience in Nephrology is a plus, but not required.

Key Responsibilities:

  • Coordinate and oversee clinical trials
  • Recruit, screen, and enroll study participants
  • Obtain informed consent and ensure participants' rights and safety are upheld throughout the study
  • Collect, process, and manage study data in compliance with GCP guidelines
  • Communicate effectively with investigators, sponsors, and regulatory agencies

Requirements:

  • Bachelor's/Associate's degree required
  • 2+ years of experience in Clinical Research
  • Experience in Nephrology is a plus
  • Phlebotomy/ECG experience required