Research Associate I
The University of Texas at Austin Staff
Research Associate I
Dell Medical School is seeking a Research Associate I. This position is temporary with an end date of June 1st, 2027, renewable based upon availability of funding, work performance, and progress toward goals.
Purpose: The Research Associate I supports scientific research by conducting experiments, collecting and analyzing data, and maintaining laboratory equipment. This role typically reports to a Principal Investigator or Senior Research Scientist and works closely with other research staff, including Research Technicians and Laboratory Assistants. The Research Associate I is responsible for ensuring the accuracy and reliability of experimental results, contributing to research publications, and assisting in the development of new research protocols.
Responsibilities
- Conduct Research Experiments
- Perform laboratory experiments under the guidance of senior researchers.
- Recruit, pre-screen, and screen potential participants utilizing approved methods and appropriate eligibility criteria. Obtain informed consent of participants following GCP guidelines.
- Collect and analyze data using various scientific techniques, including but not limited to, psychological measures, neuroimaging measures, biospecimens (blood, urine, saliva, etc.), and neurocognitive measures.
- Data entry and maintenance of accurate records of experimental procedures and results.
- Data Analysis
- 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, presentations, and manuscripts (authorship will depend on candidate's initiative and relevant contribution to work).
- Laboratory Maintenance
- Ensure the laboratory is clean, organized, and stocked with necessary supplies.
- Follow safety protocols and procedures.
- Collaboration and Communication
- Work closely with other research staff to coordinate experiments and share findings.
- Participate in team meetings and provide updates on research progress.
- Communicate effectively and professionally with external collaborators and stakeholders.
- Protocol Development
- 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.
- Marginal or Periodic Functions:
- Literature Review
- Conduct literature reviews to support ongoing research projects.
- Summarize findings and present them to the research team.
- Training and Mentorship
- Provide training and guidance to new research staff and interns.
- Assist in the onboarding process for new team members.
Knowledge/Skills/Abilities
• Meticulous in maintaining accurate records and ensuring the precision of experiments, excellent attention to detail
• Effective in conveying research findings and collaborating with team members.
• Proficient in using laboratory equipment and scientific software (i.e. Excel, RedCap, R, PsychoPy, etc.), troubleshooting experimental issues.
• Coordinating experiments with a diverse team of colleagues, participating in team discussions, supporting team goals.
• Comfortable interacting with people living with serious mental illness
• Outstanding organizational and time management skills.
Required Qualifications
Requires a Bachelor's Degree in Biology, Psychiatry, Psychology, Neuroscience, Public Health, or other related discipline with at least 1 year of research experience. Relevant education and experience may be substituted as appropriate.
Preferred Qualifications
Master's Degree and/or Bachelor's Degree with 2 years of relevant laboratory experience, including experience with specific techniques used in the research area.
- Certification as a Clinical Research Associate (CRA) from the Association of Clinical Research Professionals (ACRP) or similar certification.
- Human Subjects Research and/or Good Clinical Practice certified
- Phlebotomy licensure/certification
- Level 1 or Level 2 MRI-certified
Salary Range: $40,000 + depending on qualifications Working Conditions
• Standard office equipment
• Repetitive use of a keyboard
• Occasional weekend and evening work
• May work around biohazards
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