Medix™ | Clinical Research Coordinator

1 week ago


sacramento, United States Medix™ Full time

Job Summary:

Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity.

Key Responsibilities:

  • 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.

Qualifications:

  • 4+ years as a Clinical Research Coordinator
  • Oncology/ Cardiology experience preferred
  • Phlebotomy Certification preferred
  • Knowledge of clinical research protocols, GCP, and FDA regulations.
  • Strong organizational, communication, and multitasking skills.
  • Experience with clinical procedures and data management preferred.


This role supports advancing research by ensuring high standards of protocol adherence and participant care.



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