Clinical Research Coordinator I, Neurology

Job Summary

Works under the direction of an Investigator(s) with general supervision, to coordinate research projects. This position primarily performs patient/participant coordination, however, may conduct data management in smaller departments on as needed basis. Collects and ensures quality control of clinical or basic research data in support of multiple and/or complex research studies.

About the Role

The Okuda Neuroinnovation Lab is involved in the advancement of improvised solutions and emerging innovations that improve the delivery of medical care provided to patients. Our mission is to design and develop original devices, software solutions, and combined unique methodologies that translate into discoveries for next generation care. A significant component of our work expands current in vivo imaging capabilities. Our custom-designed platforms enable the study of 3-dimensional shape, surface texture/curvature, and structural characteristics of brain lesions, as well as anatomical structures in the context of neurological disease. These efforts enhance our diagnostic capabilities, improve clinical surveillance, and enable the effective assessment of both approved disease-modifying therapies and investigational molecules with regenerative properties.

Responsibilities

• Directly interacts with clinical research participants, as required, for the research study.
• Interacts via telephone, telehealth or in-person.
• Coverage regulatory aspects of the trial including maintaining and developing regulatory information to comply with industry standards, University policies, FDA requirements or other hospital policies.
• Coverage and schedule study procedures as per protocol.
• Screen, recruit, enroll and follow subjects according to protocol guidelines. May also assist with the consent process.
• Maintain and coordinate data collection information required for each study which may also include developing CRF's or data collection tools.
• Aid in developing and implementing research studies to include writing clinical research protocols.
• Conduct study procedures according to the protocol with proper training and check offs to maintain scope of work.
• Familiarity with research budgets to assist with or develop study budgets. May perform research billing activities, as needed, based on size of department (including linking patient calendars).
• Review research study protocols to ensure feasibility.
• Develop proficiency in the clinical trial management system, electronic medical record and other required data entry systems.
• Maintain subject level documentation.
• Performs other duties as assigned.

Qualifications

• Education: Bachelor's Degree or higher degree in medical or science related field.
• Experience: 1 year of clinical research experience. May consider additional years of experience or advanced degree in lieu of education or experience, respectively.
• Preferred: ACRP or SOCRA certification a plus.

Benefits

UT Southwestern is proud to offer a competitive and comprehensive benefits package to eligible employees. Our benefits are designed to support your overall wellbeing, and include: PPO medical plan, available day one at no cost for full-time employee-only coverage100% coverage for preventive healthcare-no copayPaid Time Off, available day oneRetirement Programs through the Teacher Retirement System of Texas (TRS)Paid Parental Leave BenefitWellness programsTuition ReimbursementPublic Service Loan Forgiveness (PSLF)

Security and EEO Statement

This position is security-sensitive and subject to Texas Education Code 51.215, which authorizes UT Southwestern to obtain criminal history record information. UT Southwestern Medical Center is committed to an educational and working environment that provides equal opportunity to all members of the University community. As an equal opportunity employer, UT Southwestern prohibits unlawful discrimination, including discrimination on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, gender expression, age, disability, genetic information, citizenship status, or veteran status.