Neurosurgery Clinical Research Lead | Study Coordination

University of Mississippi Medical Center

Jackson (MS)

On-site

USD 55,000 - 85,000

Full time

5 days ago
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Job summary

The University of Mississippi Medical Center seeks a Clinical Research Coordinator in Neurosurgery to manage and report on clinical studies within the Neurosurgery unit. You will supervise the research team, coordinate participant enrollment, and ensure data integrity for regulatory reviews.

Responsibilities include recruitment, screening, and visits; administer procedures; ensure protocol training; monitor budgets; prepare IRB documents; and maintain study records.

Qualifications

  • Bachelor's degree in health sciences or related field with at least two years of Clinical Research experience.
  • Master's degree preferred.

Responsibilities

  • Assumes responsibility for all aspects of study recruitment, screening, enrollment, and visits for eligible participants.
  • Administers study-related procedures and directs participants for hospital and physician procedures.
  • Ensures staff are knowledgeable about study protocol and delineates roles.
  • Oversees scheduling, documentation, and follow-ups with research participants.
  • Supervises patient education and referrals.
  • Monitors study budgets and billings to ensure funds and compliance with policies and regulations.
  • Prepares IRB documents and progress reports.
  • Maintains regulatory documents, files and reports.

Skills

GCP & FDA regs
Communication
Interpersonal skills
Team leadership
IRB submissions
Clinical research

Education

Bachelor’s degree in health sciences
Master’s degree preferred

Job description

The University of Mississippi Medical Center seeks a Clinical Research Coordinator in Neurosurgery to manage and report on clinical studies within the Neurosurgery unit. You will supervise the research team, coordinate participant enrollment, and ensure data integrity for regulatory reviews.

Responsibilities include recruitment, screening, and visits; administer procedures; ensure protocol training; monitor budgets; prepare IRB documents; and maintain study records.

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