Senior Clinical Research Nurse - Lead Study Coordinator

The University of Texas at Austin; Austin (TX); On-site; USD 84,000 - 105,000; Full time

Job summary

The University of Texas at Austin is seeking a Senior Clinical Research Nurse in the Department of Women's Health at Dell Medical School to coordinate and implement complex clinical studies. The role involves daily study operations, recruitment, visits, regulatory and data activities, safety reporting, and communication with sponsors and investigators.

Responsibilities include start-up, enrollment, visits, data quality, and study close-out, with collaboration across multidisciplinary teams to

Qualifications

• Bachelor's Degree in nursing or related field.
• At least 5 years of clinical research experience.
• Registered Nurse (RN) license.
• Certification in Clinical Research (CCRP or equivalent).

Responsibilities

• Coordinate and implement multiple complex clinical research studies with day-to-day management.
• Develop and maintain project plans to track study timelines and milestones.
• Identify and resolve operational issues and escalate complex matters.
• Oversee study start-up activities and regulatory documentation.
• Coordinate study close-out activities and ensure documentation is complete.
• Identify and screen potential participants, obtain informed consent, and schedule study visits.
• Monitor participants and collect required data per protocol.
• Manage study drug/device dissemination and accountability as applicable.
• Assist with data collection, specimen processing, and monitoring visits.
• Educate participants and families about study procedures.

Skills

Clinical research experience

RN license

Education

Bachelor's degree in nursing or related field

Job description

The University of Texas at Austin is seeking a Senior Clinical Research Nurse in the Department of Women's Health at Dell Medical School to coordinate and implement complex clinical studies. The role involves daily study operations, recruitment, visits, regulatory and data activities, safety reporting, and communication with sponsors and investigators.

Responsibilities include start-up, enrollment, visits, data quality, and study close-out, with collaboration across multidisciplinary teams to