1

Study Management Associate Jobs in Texas (NOW HIRING)

The Associate Clinical Project Manager will be involved and assist with the management and ... Develops and executes risk based study management process and plan according to study-specific risk ...

The Associate Clinical Project Manager will be involved and assist with the management and ... Develops and executes risk based study management process and plan according to study-specific risk ...

Materials Management Associate II

Van Horn, TX · On-site

$16.25 - $22.25/hr

Studies have shown that some people are less likely to apply to jobs unless they meet every single ... Please note this is a publicly managed inbox. Please do not include any personal medical ...

Study Manager I (3657)

Irving, TX · On-site

$80K - $96K/yr

Responsible for clinical trial management from FPFV to study close out with strict adherence to ... Working closely with the Associate Site Director/Site Director to achieve strategic goals for the ...

Summary Associate Business Manager At our Company, we grow People, Brands, and Businesses! We are ... Study/Area of Experience: Business 0-2 Years of experience in Account or Brand Management Skills ...

next page

Showing results 1-20

Study Management Associate information

See Texas salary details

$9

$35

$51

How much do study management associate jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for study management associate in Texas is $35.49, according to ZipRecruiter salary data. Most workers in this role earn between $23.47 and $46.30 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are the typical responsibilities of a Study Management Associate in a clinical research team?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What is a Study Management Associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.
Infographic showing various Study Management Associate job openings in Texas as of June 2026, with employment types broken down into 2% As Needed, 62% Full Time, 30% Part Time, 1% Temporary, and 5% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $73,829 per year, or $35.5 per hour.

$41K/yr

Full-time

Posted 19 days ago


University Of Texas at Austin rating

8.1

Company rating: 8.1 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

132nd of 536 rated colleges and universities


Job description

Job Posting Title:
Research Associate I
----
Hiring Department:
Department of Psychiatry
----
Position Open To:
All Applicants
----
Weekly Scheduled Hours:
40
----
FLSA Status:
Exempt from FLSA
----
Earliest Start Date:
Jun 01, 2026
----
Position Duration:
Expected to Continue Until Aug 31, 2027
----
Location:
AUSTIN, TX
----
Job Details:
General Notes
The Department of Psychiatry and Behavioral Sciences at the Dell Medical School is seeking a Research Associate I. This is a grant funded position with an end date of 8/31/2027, renewable based upon availability of funding, work performance, and progress toward research goals.
This position will provide research assistance/support for research projects in the Department of Psychiatry at UT Austin working as part of a team of faculty, staff, graduate students, and undergraduate assistants.
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
Participant Assessments
  • Reviews medical records.
  • Conducts screenings for study recruitment.
  • Executes data collection procedure and assessment.
  • Assists with subject recruitment.

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 and presentations.
  • Assist with manuscripts and publications by drafting sections, reviewing content, and ensuring adherence to publication guidelines.

Study Management
  • Helps with subject management, including phone calls and general coordination to schedule patients for study visits and follow-ups, and reimbursement.
  • Work closely with Principal Investigators (PIs), clinicians, and other research staff to facilitate study operations.
  • Work both independently and as part of a team to achieve project goals. Perform administrative and coordinating tasks pertaining to study management.

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 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:
Training and Mentorship
• Provide training and guidance to new research staff and interns.
• Assist in the onboarding process for new team members.
Grant Writing Support
• 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.
KNOWLEDGE/SKILLS/ABILITIES
• 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.
EDUCATION & EXPERIENCE
MINIMUM QUALIFICATIONS:
Bachelor's degree in a scientific, engineering or technical field. Basic engineering and/or scientific equipment ordinarily used in college laboratory work.
Relevant education and experience may be substituted as appropriate.
According to Executive Order No. GA-48 of the State of Texas: for all positions that research, work on, or have access to critical infrastructure as defined in Section 117.001(2), Business and Commerce Code, it is required that both candidates for employment and employees have the ability to maintain the security or integrity of the infrastructure.
PREFERRED QUALIFICATIONS:
Experience with projects involving Human subject research.
Bilingual in English and Spanish preferred.
Experience with REDCap.
LICENSES, REGISTRATIONS OR CERTIFICATIONS
REQUIRED:
• None.
Salary Range
$41,000 + depending on qualifications
WORKING ENVIRONMENT/EQUIPMENT
• Standard office equipment
• Repetitive use of a keyboard
Required Materials
  • Resume/CV
  • 3 work references with their contact information; at least one reference should be from a supervisor
  • Letter of interest

Important for applicants who are NOT current university employees or contingent workers: 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; you will be able to multi-select additional files. Before submitting your online job application, ensure that ALL Required Materials have been uploaded. Once your job application has been submitted, you cannot make changes.
Important for Current university employees and contingent workers: 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 questions presented to upload any additional Required Materials (letter of interest, references, etc.) that were noted above.
Employment Eligibility:
Regular staff who have been employed in their current position for the last six continuous months are eligible for openings being recruited for through University-Wide or Open Recruiting, to include both promotional opportunities and lateral transfers. Staff who are promotion/transfer eligible may apply for positions without supervisor approval.
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.
Background Checks:
A criminal history background check will be required for finalist(s) under consideration for this position.
Equal Opportunity Employer:
The University of Texas at Austin, as an equal opportunity/affirmative action employer, complies with all applicable federal and state laws regarding nondiscrimination and affirmative action. 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.
Pay Transparency:
The University of Texas at Austin will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. 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.
Employment Eligibility Verification:
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.
----
E-Verify:
The University of Texas at Austin use E-Verify to check the work authorization of all new hires effective May 2015. The university's company ID number for purposes of E-Verify is 854197. For more information about E-Verify, please see the following:
  • E-Verify Poster (English and Spanish) [PDF]
  • Right to Work Poster (English) [PDF]
  • Right to Work Poster (Spanish) [PDF]

----
Compliance:
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). If this position is identified a Campus Security Authority (Clery Act), you will be notified and provided resources for reporting. Responsible employees under Title IX are defined and outlined in HOP-3031.
The Clery Act requires all prospective employees be notified of the availability of the Annual Security and Fire Safety report. You may access the most recent report here or obtain a copy at University Compliance Services, 1616 Guadalupe Street, UTA 2.206, Austin, Texas 78701.

What University Of Texas at Austin employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom