Research Trials Coordinator

3 weeks ago


Sacramento, California, United States Medix™ Full time

Medix™

Research Trials Coordinator

We are seeking an experienced Research Trials Coordinator to join our team at Medix™. This role will play a critical part in advancing research by ensuring high standards of protocol adherence and participant care.

About the Job:

The Research Trials Coordinator is responsible for facilitating site initiation and sponsor-required training for clinical protocols. They will also be responsible for dispensing study medications, processing and shipping lab specimens, and conducting informed consent processes.

Key Responsibilities:

  • Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies.
  • Facilitate site initiation and sponsor-required training for clinical protocols.
  • Dispense study medications and coordinate with pharmacy staff as needed.
  • Process and ship lab specimens in compliance with federal regulations.
  • Conduct informed consent processes, ensuring proper documentation and compliance.
  • Schedule and oversee study visits, tests, and procedures per protocol requirements.
  • Accurately collect and report data, maintaining research subject charts and source documents.
  • Perform or coordinate clinical procedures (e.g., blood draws, ECGs) with appropriate training.
  • Report adverse events, protocol deviations, and violations to study sponsors and IRBs.
  • Prepare and submit regulatory documents, including IRB applications and consent forms.
  • Support participant recruitment, screening, enrollment, and retention.
  • Serve as a liaison between participants, investigators, sponsors, and regulatory bodies.
  • Assist in sponsor monitoring visits and audits, resolving findings promptly.

Salary Range: $60,000 - $80,000 per year



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