Research Associate I

The University of Texas at Austin•Austin, UT

3d•Onsite

About The Position

Dell Medical School is seeking a Research Associate I. This is a state-funded position with an end date of 8/31/2027 that is renewable for another year. The Senior Clinical Research Coordinator (Senior CRC) independently coordinates complex interventional trials and multi‑site studies under a Principal Investigator (PI) and/or Research Operations leader, ensuring protocol fidelity, participant safety, regulatory compliance (ICH‑GCP; FDA 21 CFR 50/56), HIPAA adherence, high‑quality data, and monitoring/audit readiness. The Senior CRC leads screening and informed consent; plans and conducts study visits; manages investigational product and specimen workflows; performs AE/SAE reporting; and maintains IRB submissions, continuing reviews, and amendments. Senior CRCs also mentor junior coordinators and contribute to feasibility, budgets, and enrollment strategies.

Requirements

Requires a Bachelor's Degree in psychology, social work, neuroscience, engineering, computer science, or another STEM-related field with relevant research experience.
Relevant education and experience may be substituted as appropriate.
Addressing individuals and health-related information with a high degree of sensitivity and confidentiality in various delicate, formal or urgent situations.
Outstanding organizational and time-management skills.
Interpreting experimental results, identifying trends in data, troubleshooting experimental issues.
Meticulous in maintaining accurate records and ensuring the precision of experiments.
Effective in conveying research findings and collaborating with team members.
Proficient in using laboratory equipment and scientific software.
Coordinating experiments with colleagues, participating in team discussions, supporting team goals.
A criminal history background check will be required for finalist(s) under consideration for this position.
If hired, you will be required to complete the federal Employment Eligibility Verification I-9 form.
You will be required to present acceptable and original documents to prove your identity and authorization to work in the United States.
Documents need to be presented no later than the third day of employment.
Failure to do so will result in loss of employment at the university.

Nice To Haves

Master's Degree in with at least 2 year(s) of research experience actively working in data collection in a psychology, psychiatry, social work, counseling, or human subjects biomedical research laboratory.
Previous experience with MRI and/or electroencephalogram acquisition or analysis
Previous experience in standardized behavioral/neuropsychological assessments and clinical research
Certification as a Clinical Research Associate (CRA) from the Association of Clinical Research Professionals (ACRP) or similar certification.

Responsibilities

Perform laboratory experiments under the guidance of senior researchers.
Collect and analyze data through clinical interviews, behavioral measures, and other techniques.
Maintain accurate records of experimental procedures and results.
Analyze research data using statistical software and tools.
Interpret results and prepare reports for review by senior researchers.
Assist in the preparation of research publications and presentations.
Assist with manuscripts and publications by drafting sections, reviewing content, and ensuring adherence to publication guidelines.
Maintain and calibrate laboratory equipment.
Ensure the laboratory is clean, organized, and stocked with necessary supplies.
Follow safety protocols and procedures.
Work closely with other research staff to coordinate experiments and share findings.
Participate in team meetings and provide updates on research progress.
Communicate effectively with external collaborators and stakeholders.
Assist in the development and optimization of research protocols.
Review and update standard operating procedures (SOPs) as needed.
Ensure compliance with regulatory and ethical guidelines.
Assist with IRB submission and management by preparing necessary documentation, coordinating with IRB representatives, and ensuring timely submission and approval.
Conduct literature reviews to support ongoing research projects.
Summarize findings and present them to the research team.
Provide training and guidance to new research staff and interns.
Assist in the onboarding process for new team members.
Assist in the preparation of grant proposals and funding applications.
Provide data and information to support grant submissions.
Adheres to internal controls and reporting structure.
Performs related duties as required.