Clinical Research Assistant 182825 Job at Medix™, Fort Lauderdale, FL

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  • Medix™
  • Fort Lauderdale, FL

Job Description

Key Responsibilities:

  • Assist with the planning, implementation, and coordination of clinical research studies.
  • Recruit, screen, and enroll study participants based on study protocols.
  • Schedule and conduct study visits, follow-ups, and patient assessments.
  • Maintain accurate and up-to-date source documents, case report forms (CRFs), and study records.
  • Assist in obtaining informed consent from study participants in accordance with ethical guidelines.
  • Collect, process, and ship biological samples as required by the protocol.
  • Communicate with institutional review boards (IRBs), sponsors, and other stakeholders.
  • Ensure compliance with all applicable regulatory requirements and protocols.
  • Enter and manage data using electronic data capture systems (EDC).
  • Assist with the preparation of study-related documentation, including reports, SOPs, and training materials.
  • Support monitoring visits, audits, and inspections

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