Neuro Research Coordinator - Clinical Trials in Austin

Ascension

Austin (TX)

On-site

USD 55,000 - 85,000

Full time

36 hours ago
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Benefits offered by this job

Health coverage
403(b) retirement plan
PTO and holidays
Tuition reimbursement
Employee assistance program
Parental leave
Family benefits
Pet insurance
Transportation savings

Job summary

Ascension in Austin, TX seeks a Clinical Research Coordinator in the Neurological Surgery department. This full-time role (Mon-Fri) supports protocol planning, participant recruitment and IRB compliance, collaborating with investigators and research staff to monitor progress and ensure safety.

You will prepare materials, coordinate communications, and help manage audits and regulatory requirements, contributing to a well-organized research program within a leading Catholic health system.

Qualifications

  • None required credential.
  • PRIM&R Certification or Research Professional preferred.

Responsibilities

  • Collaborates with PI, sponsor and research staff to plan, conduct and evaluate project protocols.
  • Assists with recruitment, scheduling, and monitoring of research participants and handles adverse events and audits.
  • Coordinates preparation and delivery of departmental communications, presentations and materials.
  • Ensures compliance with regulations and responds to audits as needed.
  • Coordinates activities for the IRB and maintains required documents and training materials.
  • Supports documentation, presentations, files and databases for IRB compliance.

Education

High School diploma equivalency with 2 years of cumulative experience OR Associate's degree/Technical degree OR 4 years of applicable cumulative job specific experience required.

Job description

Ascension in Austin, TX seeks a Clinical Research Coordinator in the Neurological Surgery department. This full-time role (Mon-Fri) supports protocol planning, participant recruitment and IRB compliance, collaborating with investigators and research staff to monitor progress and ensure safety.

You will prepare materials, coordinate communications, and help manage audits and regulatory requirements, contributing to a well-organized research program within a leading Catholic health system.

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