Clinical Research Associate II - Neuroimmunology Trials

utaustin; Austin (TX); On-site; USD 43,000 - 53,000; Full time

Job summary

University of Texas at Austin is seeking a Clinical Research Associate II to support clinical research under the Department of Neurology, primarily at the MS and Neuroimmunology Center. The role emphasizes scheduling, participant interaction, study administration, and regulatory compliance.

The position focuses on coordinating funded studies, data collection, and collaboration with PIs, sponsors, and study staff, with opportunities to contribute to budget planning and IRB activities.

Qualifications

• Requires a Bachelor’s Degree in Neuroscience, Psychology, life sciences or related field with at least 3 years of experience.
• At least 3 years of relevant experience in clinical research.
• Relevant education and experience may be substituted as appropriate.

Responsibilities

• Support recruitment of research participants, screening, informed consent, and data collection.
• Monitor site recruitment progress and ensure protocol adherence and accurate data collection.
• Maintain project timelines and coordinate with PIs to meet milestones.
• Assist in preparing reports, presentations, and manuscripts for dissemination.
• Collaborate with PIs to refine study protocols and procedures.
• Assist with IRB submissions and ongoing regulatory documentation.

Skills

Communication

Project management

Attention to detail

Independent study management

Discretion with sensitive information

Adaptability

Education

Bachelor’s degree (Neuroscience, Psychology, life sciences or related)

Master’s degree (Neuroscience, Psychology, life sciences or related)

Job description

University of Texas at Austin is seeking a Clinical Research Associate II to support clinical research under the Department of Neurology, primarily at the MS and Neuroimmunology Center. The role emphasizes scheduling, participant interaction, study administration, and regulatory compliance.

The position focuses on coordinating funded studies, data collection, and collaboration with PIs, sponsors, and study staff, with opportunities to contribute to budget planning and IRB activities.