Neurosurgery Clinical Research Coordinator

ummc

Jackson (MS)

On-site

USD 45,000 - 65,000

Full time

4 days ago
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Job summary

UMMC is seeking a Clinical Research Coordinator for Neurosurgery to oversee recruitment, screening, enrollment and visits for studies on the Main Campus in Jackson. You will ensure protocol adherence, manage documentation and liaise with investigators and sponsors.

Responsibilities include maintaining regulatory files, preparing IRB materials, and supervising study staff. A health-sciences background and CR experience are required.

Qualifications

  • Bachelor's degree in health sciences or related field required.
  • At least 2 years of clinical research experience required.
  • Master's degree preferred.

Responsibilities

  • Manages recruitment, screening, enrollment, and visits for eligible participants.
  • Ensures staff are knowledgeable about study protocol and delineates roles/responsibilities.
  • Oversees scheduling, documentation, and follow-ups with participants; supervises education and referrals.
  • Monitors study budgets and billing for compliance with policies and regulations.
  • Communicates with investigators, sponsors, regulatory agencies, and compliance personnel on study matters.
  • Prepares IRB documents and progress reports; maintains regulatory files and reports.
  • Duties may be adjusted by management as needed.

Skills

Good clinical practice
FDA regulations
Oral and written communication
Interpersonal skills
Team leadership
IRB submissions/amendments
Documentation and records
Organizational skills

Education

Bachelor's degree in health sciences or related field
Clinical Research experience 2+ years
Master's degree preferred

Job description

UMMC is seeking a Clinical Research Coordinator for Neurosurgery to oversee recruitment, screening, enrollment and visits for studies on the Main Campus in Jackson. You will ensure protocol adherence, manage documentation and liaise with investigators and sponsors.

Responsibilities include maintaining regulatory files, preparing IRB materials, and supervising study staff. A health-sciences background and CR experience are required.

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