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How much do part time clinical research rater jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for part time clinical research rater in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a part time clinical research rater?

A Part Time Clinical Research Rater is a professional who assists in clinical research studies by administering assessments, collecting data, and evaluating participants under the supervision of a research team. Their primary responsibilities include conducting interviews, scoring standardized tests, and documenting findings accurately. Working part-time, they often have flexible hours and may work on multiple studies at once. This role is important for ensuring data quality and reliability in clinical trials, particularly in areas like psychology, psychiatry, and neurology.

What are the key skills and qualifications needed to thrive as a part time clinical research rater?

To thrive as a Part Time Clinical Research Rater, you need a background in psychology, nursing, or a related field and experience with clinical assessments or research protocols. Familiarity with electronic data capture systems, standardized rating scales (e.g., HAM-D, MADRS), and basic statistical software is typically required. Attention to detail, strong organizational skills, and effective communication help ensure accuracy and integrity in data collection. These skills are crucial for delivering reliable research results and maintaining high-quality study standards.

What is the difference between Part Time Clinical Research Rater vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Research RaterPart Time Clinical Research Coordinator
CredentialsTypically requires a high school diploma or equivalent; some roles prefer healthcare or research experienceRequires a bachelor's degree in health sciences or related field; certification may be preferred
Work EnvironmentRemote or flexible settings, focusing on assessments and data collectionClinical sites or research facilities, overseeing study procedures and participant management
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for data collectionEmployed by hospitals, research institutions, and pharmaceutical companies to coordinate studies

While both roles support clinical research, Part Time Clinical Research Raters primarily focus on evaluating participants' responses and data collection remotely, whereas Part Time Clinical Research Coordinators manage study logistics and participant interactions on-site. The roles differ in responsibilities, required credentials, and work environment, but both contribute to the successful conduct of clinical trials.

How does a part time clinical research rater typically collaborate with other members of a research team?

As a Part Time Clinical Research Rater, you will work closely with clinical coordinators, principal investigators, and other raters to ensure consistent and accurate data collection. Collaboration often involves regular meetings to discuss study protocols, review rating scales, and resolve discrepancies in assessments. Effective communication is key, as you may need to clarify procedures, share observations, and update the team on participant progress. This teamwork ensures the integrity of study data and contributes to the overall success of clinical trials.
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Part Time Clinical Research Rater jobs near you
Infographic showing various Part Time Clinical Research Rater job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Research Assistant Must Be Bilingual English-Spanish

Angel City VA

Los Angeles, CA • On-site

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

Title: Part time Clinical Research assistant
Job Summary:
The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, blood pressure, urine collection, draw labs
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
• Office/administrative tasks assigned ie: resupplying exam rooms, ordering office supplies, answering phone calls, etc.
Education/Experience/Skills:
• High school graduate or equivalent. Bac
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to clearly communicate both orally and verbally.
• Prior experience in healthcare, research, or clinical settings is a plus.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.

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