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Assistant Clinical Research Rater Jobs in Austin, TX

Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours ... Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral ...

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Assistant Clinical Research Rater information

See Austin, TX salary details

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How much do assistant clinical research rater jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for assistant clinical research rater in Austin, TX is $20.05, according to ZipRecruiter salary data. Most workers in this role earn between $16.44 and $23.12 per hour, depending on experience, location, and employer.

What is the difference between Assistant Clinical Research Rater vs Clinical Research Coordinator?

AspectAssistant Clinical Research RaterClinical Research Coordinator
Required CredentialsHigh school diploma or equivalent; some roles may require a bachelor's degreeBachelor's degree in health sciences or related field; certification often preferred
Work EnvironmentRemote or in clinical settings; primarily data review and assessmentsClinical sites; managing study logistics and participant coordination
Employer & Industry UsageResearch organizations, pharmaceutical companies, universitiesHospitals, research institutions, pharmaceutical companies
Common Search & Comparison IntentUnderstanding entry-level roles in clinical researchManaging clinical trials and participant interactions

The Assistant Clinical Research Rater typically focuses on reviewing and assessing data, often working remotely, with minimal direct patient interaction. In contrast, the Clinical Research Coordinator manages the overall conduct of clinical trials, including participant recruitment and site management. Both roles are essential in clinical research but differ in responsibilities, required credentials, and work environment.

What are the most commonly searched types of Clinical Research Rater jobs in Austin, TX?

The most popular types of Clinical Research Rater jobs in Austin, TX are:

What cities near Austin, TX are hiring for Assistant Clinical Research Rater jobs?

Cities near Austin, TX with the most Assistant Clinical Research Rater job openings:

Infographic showing various Assistant Clinical Research Rater job openings in Austin, TX as of August 2026, with employment types broken down into 6% As Needed, 65% Full Time, 17% Part Time, 6% Temporary, and 6% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $41,710 per year, or $20.1 per hour.

Clinical Research Assistant

Austin, TX • On-site

Pinnacle Clinical Research
Health Care and Social Assistance • 201 - 500 employees

Full-time

Re-posted 5 days ago


Job description

Summary: Assists the Clinical Research Coordinator and the principal investigator with administering activities to facilitate clinical research, which may include working with an affiliate or collaborating research sites. Exercises judgment within the allowable limits defined within clinical trials protocols, standard operating procedures, and under the direction from the study Investigator and supervisor. Always maintains subject and document confidentiality, understands and complies with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards (IRB), and institutional policies and procedures by performing the following duties.

Duties and Responsibilities:

  • Assists with the creation and completion of study related documents and new study preparation.
  • Assists with the completion of regulatory submissions and maintains regulatory files as directed.
  • Acts as a secondary liaison with sponsors.
  • Assists with the preparation for study monitor visits as directed.
  • Completes case report forms as directed.
  • Creates reports as requested.
  • Completes study directed assessments with patients to include, but not limited to adverse events, test article (TA) handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessment.
  • Assists with subject screening and recruitment as directed.
  • Updates Clinical Trial Management Software (CTMS) as directed.
  • Coordinates multiple projects with competing priorities and deadlines, as needed based on clinical trial protocol directives and study volume.
  • Interacts with internal and external personnel to include, but not limited to physicians, nurses, administration staff, industry sponsor representatives, central laboratory/imaging personnel, and clinical trial patients.


Duties, responsibilities, and activities may change, or new ones assigned at any time.


Education Experience:

High school diploma or general education degree (GED); or two to four years related experience and/or training; or equivalent combination of education and experience.

Certificates and Licenses:

  • Clinical research certification preferred

Knowledge, Skills, and Other Abilities:

  • Ability to demonstrate competence in oral and written communication
  • Bilingual (English/Spanish) required
  • Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor
  • Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
  • Medical knowledge, including medical terminology
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization.
  • Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems.

Work Environment and Physical demands:

The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Work is performed in an office/laboratory and/or a clinical environment.
  • Exposure to biological fluids and/or bloodborne pathogens. 
  • Personal protective equipment required such as protective eyewear, garments, and gloves.
  • Occasional travel may be required domestic and/or international.
  • Ability to work in an upright and/or stationary position for 6-10 hours per day.
  • Frequent mobility required.
  • Occasional squatting, kneeling, or bending.
  • Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.