Clinical Research Monitoring (CRA)
University of Texas at Austin
Clinical Research Associate I ----
Department of Psychiatry ----
Immediately ----
General Notes This is a grant-funded position with an end date of September 1, 2027, renewable based upon availability of funding, work performance, and progress toward research goals.
Purpose The Clinical Research Associate I (CRA I) is responsible for assisting in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and study protocols. Key responsibilities include site management, data collection, and ensuring the integrity of clinical data.
The Clinical Research Associate I will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI). This role may coordinate the data collection and operations of multiple concurrent clinical research studies under the guidelines of research protocols, The University of Texas at Austin, and regulatory agency policies.
and the ability to prioritize and complete multiple projects within established deadlines.
Responsibilities Site Management & Study Execution
Conduct site initiation, monitoring, and close-out visits while managing participant recruitment, screening, and enrollment to ensure protocol adherence, regulatory compliance, and successful study execution.
Ensure compliance with study protocols and regulatory requirements.
Manage site performance and resolve issues.
Administer questionnaires, collect medical history, and perform study procedures.
Data Collection & Management
Collect and verify data from clinical sites.
Ensure accurate and timely data entry into electronic data capture systems (e.g., Review and resolve data queries.
Assist with manuscript and grant preparation, including opportunities for authorship.
Maintain and update study databases and data collection forms.
Regulatory Compliance & Oversight
Ensure adherence to Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
Facilitate institutional review board (IRB) applications, submissions, and updates across multiple sites.
Prepare and maintain regulatory documents.
Evaluate medical records and perform screenings to identify eligible study participants.
Assist in training new site staff and research team members.
Adhere to internal controls and reporting structure.
Bachelor's degree in life sciences, nursing, or a related field
One year of relevant clinical research experience
Experience with electronic data capture systems (e.g., Master's degree in life sciences, nursing, or a related field with at least two years of clinical research experience, preferably involving pediatric or neurodevelopmental populations
Experience with statistical software (e.g., R, SAS, SPSS)
Experience presenting research findings or contributing to publications
Completion of Human Subjects Protection Training
Experience working with children and families affected by neurodevelopmental disorders
Ability to abstract data from medical records and manage complex databases
Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP)
May work around standard office conditions
Occasional weekend, overtime, and evening work to meet deadlines
Occasional interstate, intrastate, and international travel
This position will be assigned on-campus with an expectation to report to work on-site during the scheduled work week.
Required Materials
~ You will be prompted to submit your resume the first time you apply, then you will be provided an option to upload a new Resume for subsequent applications. Any additional Required Materials (letter of interest, references, etc.) will be uploaded in the Application Questions section; Before submitting your online job application, ensure thatALLRequired Materials have been uploaded. Once your job application has been submitted, you cannot make changes.
As a current university employee or contingent worker, you MUST apply within Workday by searching for Find UT Jobs. If you are a current University employee, log-in to Workday, navigate to your Worker Profile, click the Career link in the left hand navigation menu and then update the sections in your Professional Profile before you apply. This information will be pulled in to your application. The application is one page and you will be prompted to upload your resume. In addition, you must respond to the application questionspresented to upload any additional Required Materials (letter of interest, references, etc.) Retirement Plan Eligibility:
The retirement plan for this position is Teacher Retirement System of Texas (TRS), subject to the position being at least 20 hours per week and at least 135 days in length. ----
A criminal history background check will be required for finalist(s) under consideration for this position.
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The University is committed to a policy of equal opportunity for all persons and does not discriminate on the basis of race, color, national origin, age, marital status, sex, sexual orientation, gender identity, gender expression, disability, religion, or veteran status in employment, educational programs and activities, and admissions.
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However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
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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. E-Verify Poster (English and Spanish) [PDF]
Right to Work Poster (English) [PDF]
Right to Work Poster (Spanish) [PDF]
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Employees may be required to report violations of law under Title IX and the Jeanne Clery Disclosure of Campus Security Policy and Crime Statistics Act (Clery Act). The Clery Act requires all prospective employees be notified of the availability of the Annual Security and Fire Safety report.
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