Research Coordinator

Lifelancer
Round Rock, TX
Category Research
Job Description
The Research Coordinator advocates for patient safety and protocol integrity, adheres to patient care standards, and communicates effectively to ensure effective conduct of clinical trials and quality patient care.

Requirements

  • Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research
  • Provides protocol specific education to clinical staff
  • Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient
  • Assesses ongoing consent through discussions with patients and reinforcement of education
  • Ensures timely re-consenting as needed by the physician investigator
  • Demonstrates understanding of tiered consent process when optional correlative studies are involved
  • Collaborates with the investigator to ascertain study patient eligibility for a clinical trial, including documentation of criteria specified in the protocol
  • Coordinates, schedules, and ensures timely completion of protocol-required events and other requirements
  • Documents all patient encounters in the legal medical record per licensure and institutional requirements
  • Maintains specified study documents in the Research Coordinator files
  • Adheres to the data management plan per NEXT SOPs and sponsor data management plan
  • Enters data into electronic data capture for SAEs as appropriate

Benefits

  • Health and welfare benefits
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