Perioperative Neuroimaging Research Coordinator

Stanford University

Palo Alto (CA)

On-site

USD 70,000 - 85,000

Full time

14 days+
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Job summary

Stanford University’s Purdon Lab seeks a Clinical Research Coordinator Associate (Fixed-term 2 years) to coordinate perioperative clinical studies, including preoperative, operating room, and PACU activities. The role involves data collection, EEG/MRI processing, neuropsychological testing, and regulatory compliance within Stanford hospital settings.

The CRCA will manage study documentation, recruit participants, and coordinate budgets and communications with sponsors.

Qualifications

  • Strong interpersonal skills.
  • Proficiency with Microsoft Office.
  • Knowledge of medical terminology.

Responsibilities

  • Serve as primary contact with research participants, sponsors, and regulatory agencies.
  • Determine eligibility of and gather consent from study participants according to protocol.
  • Coordinate collection of study specimens and processing.
  • Collect and manage patient and laboratory data for clinical research projects.
  • Ensure compliance with research protocols and regulatory submissions.
  • Assemble study kits for visits and monitor scheduling of procedures.
  • Monitor expenditures and adherence to study budgets.
  • Interact with the principal investigator to ensure patient safety.
  • Ensure essential documentation and recording of data per requirements.
  • Participate in monitor visits and regulatory audits.

Skills

Interpersonal skills
Microsoft Office
Medical terminology

Education

Two-year college degree + 2 years related experience
Bachelor’s degree in related field

Job description

Stanford University’s Purdon Lab seeks a Clinical Research Coordinator Associate (Fixed-term 2 years) to coordinate perioperative clinical studies, including preoperative, operating room, and PACU activities. The role involves data collection, EEG/MRI processing, neuropsychological testing, and regulatory compliance within Stanford hospital settings.

The CRCA will manage study documentation, recruit participants, and coordinate budgets and communications with sponsors.

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