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

  • Identifies primary and secondary study objectives and outcome measures
  • Adheres to applicable federal, state, and institutional regulations, policies, and procedures related to clinical research
  • Provides protocol specific education to clinical staff
  • Provides timely, accurate, and complete reporting of serious adverse events, unanticipated problems, deviations, violations, and noncompliance to the IRB and sponsor
  • Informed patient about research study and ensures informed consent
  • Collaborates with the investigator to determine disease response as defined by the protocol and communicates findings to the study team and other care providers
  • Maintains the privacy and confidentiality of patients' source documents
  • Participates in the development of approved source documents, templates, or forms
  • Ensures that relevant data from source documents are abstracted and entered into CRFs in a timely and accurate manner
  • Participates in quality control activities to ensure data integrity, including timely responses to database or sponsor queries

Benefits

  • Health and welfare and/or other benefits
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