Clinical Research Associate I

* Conducts site initiation, monitoring, and close-out visits.* Ensures compliance with study protocols and regulatory requirements.* Manages site performance and resolves issues.* Supports participant coordination and visit management, including scheduling, visit reminders, and reimbursement processes under PI or senior staff oversight.* Coordinates with clinical staff for specimen collection and protocol-required procedures.* Conducts literature reviews to support study design and protocol development.* Assists in the training of new site staff and research team members.* Participates in internal and external audits.* Supports the development of study protocols and case report forms.* Attends conferences and workshops to stay updated on industry trends.* Performs other tasks as assigned to support research team and project goals* Adheres to internal controls and reporting structure.* Performs related duties as required.* Double-checks work for errors, maintains organized records, and follows detailed procedures.* Writes clear and concise reports, actively listens to others, and presents information effectively.* Analyzes information, develops solutions, and implements corrective actions.* Shares information, supports team decisions, and contributes to team success.* Prioritizes tasks, sets realistic deadlines, and uses time efficiently.* Basic proficiency in Microsoft Office Suite (Word, Excel, Outlook). Familiarity with data entry platforms such as REDCap or ability and willingness to learn.* Demonstrated ability to collaborate effectively with participants, clinical staff, and research teams.* Detail-oriented with strong time management; able to follow protocols and maintain regulatory compliance.* Requires a Bachelor's Degree in life sciences, nursing, or a related field.* 1 year of relevant clinical research experience.* Relevant education and experience may be substituted as appropriate* Master's Degree in life sciences, nursing, or a related field. with at least 2 year(s) of experience in clinical research experience.* Experience in research or healthcare environment (e.g., internships, volunteer roles, or academic projects).* Good Clinical Practice (GCP) Certification: Demonstrates understanding of GCP guidelines.* Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP).* CITI Human Subjects Research Training.* GCP (Good Clinical Practice) certification.**Start Here, Change the World**At The University of Texas at Austin, tradition meets innovation in the heart of a city that frequents lists of the best places to live and work. Named by Forbes as one of America's Best Large Employers for the sixth year in a row in 2025, UT offers both a dynamic work environment and a gateway to vibrant local culture. Whether you're at the forefront of the student experience, conducting world-changing research or supporting the engine that drives Texas’ flagship university, working at UT means making a lasting impact on our city, our state and our world.Our more than 20,000 faculty and staff empower 55,000+ students to challenge ideas, pursue passions and shape their futures. Joining UT, you’ll become part of a community dedicated to making a meaningful impact on campus and throughout the world.Please see our .**Comments and Inquiries:**Email comments to View email address on click.appcast.io. For questions or concerns regarding equal opportunity only, contact .Additional information for applicants can be found on the Human Resources web page: . For more job information, call the Human Resource Service Center at View phone number on click.appcast.io, or toll-free at View phone number on click.appcast.io. #J-18808-Ljbffr The University of Texas at Austin