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Full Time Clinical Research Rater Jobs in California

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Full Time Clinical Research Rater information

What is a full time clinical research rater?

Full Time Clinical Research Raters are professionals who assess and document the progress, symptoms, and responses of patients participating in clinical research studies. They use standardized rating scales, interviews, and questionnaires to collect accurate data that helps determine the effectiveness and safety of new treatments or interventions. These raters play a vital role in ensuring the integrity and quality of clinical trial data, often working closely with clinicians, researchers, and study coordinators. Their responsibilities also include adhering to study protocols, maintaining patient confidentiality, and ensuring compliance with regulatory standards.

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

Success as a Full Time Clinical Research Rater requires a background in psychology, neuroscience, or a related field, along with experience in clinical assessments and data collection. Familiarity with standardized rating scales, clinical trial databases, and regulatory compliance systems like Good Clinical Practice (GCP) certification is typically expected. Strong attention to detail, interpersonal communication, and objective judgment are crucial soft skills for accurate participant evaluation and collaboration with research teams. These competencies ensure reliable data collection, regulatory adherence, and the integrity of clinical research outcomes.

What are some typical challenges a full time clinical research rater may encounter, and how can they be managed?

Full Time Clinical Research Raters often face challenges such as managing large volumes of patient assessments, maintaining objectivity during subjective ratings, and adhering to strict study protocols. Balancing accuracy with efficiency is key, especially when dealing with sensitive patient information and tight study timelines. Collaborating closely with investigators and other research staff, participating in regular trainings, and using standardized rating tools can help ensure consistency and reliability in data collection.

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

AspectFull Time Clinical Research RaterPart Time Clinical Research Rater
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CertificationsOften requires relevant healthcare or research certificationsMay require similar certifications but less emphasis
Work EnvironmentFull-time employment in research facilities or remotePart-time roles, flexible locations
Employer UsageMajor research organizations, pharmaceutical companiesFreelance or contract research organizations

The main difference between a Full Time Clinical Research Rater and a Part Time Clinical Research Rater lies in work hours, certification emphasis, and employment type. Full-time roles offer consistent hours and benefits, while part-time positions provide flexibility. Both roles involve evaluating clinical data, but full-time positions are more integrated into research teams.

What are the most commonly searched types of Clinical Research Rater jobs in California?

The most popular types of Clinical Research Rater jobs in California are:

What are popular job titles related to Full Time Clinical Research Rater jobs in California?

For Full Time Clinical Research Rater jobs in California, the most frequently searched job titles are:

What job categories do people searching Full Time Clinical Research Rater jobs in California look for?

The top searched job categories for Full Time Clinical Research Rater jobs in California are:

What cities in California are hiring for Full Time Clinical Research Rater jobs?

Cities in California with the most Full Time Clinical Research Rater job openings:

Full Time Clinical Research Rater jobs near you
Infographic showing various Full Time Clinical Research Rater job openings in California as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical Research Supervisor

Retinal Consultants Medical Group

Chico, CA • On-site

$32 - $50/hr

Full-time

Posted 18 days ago

Job description

Description
Come and join our team! We are a local growing private medical practice specializing in the diagnosis and treatment of patients with diseases of the retina and vitreous. We are looking for individuals who would like to establish a career in healthcare working with nationally recognized physicians. We provide on the job training giving you the ability to grow and advance your skills along with gaining innovative knowledge. Established in 1977, we have locations all over Northern California including Sacramento, Grass Valley, Roseville, Stockton, Modesto, Merced, Fairfield, Elk Grove, Folsom, Yuba City and Chico. Our physicians are nationally known, and we continue to be on the leading edge of retina care by utilizing the latest equipment and both participating in and designing new clinical trials to advance the state of care for retinal diseases. Join 250+ other team members working for our nationally recognized retina specialty practice in a fast paced, high volume medical office.
The research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.
We seek a full-time Clinical Research Supervisor to support our clinical research department. Although you must be able to work independently, you will be working directly with physicians, patients, research coordinators, clinical and business office staff and with pharmaceutical sponsor representatives to correctly and efficiently execute clinical research protocols. Collaboration and being a team player are essential to the success of this role.
Responsibilities:
  • Responsible for overseeing day-to-day research activities, program operations, and administration.
  • Ensures clinical research studies are conducted efficiently and in compliance with FDA and GCP guidelines.
  • Maintains current knowledge of Federal, State, and institutional guidelines and requirements governing research.
  • Assists Department Regulatory Coordinator with the preparation and maintenance of regulatory documentation for submission for review by the Institutional Review Board (IRB) and other required review committees. This includes new, renewals, amendments, modifications, and revisions of protocols, descriptions of study, investigational drug information, HIPAA documentation and development of consent forms consistent with legal, Human Subjects Review Committee and Department of Health and Human Services (DHHS) requirements.
  • Assists the Clinical Trial Manager and Principal Investigators in providing information to sponsors and vendors during study startup, conduct and closeout process.
  • Ensures the study site operates at RCA expected levels of service, timeliness, and accuracy.\
  • Supervises clinical research staff by setting goals, conducting regular meetings, and monitoring performances.
  • Assists the Clinical Trials Director with study staff hiring, training, and annual evaluations.
  • Updates site study assignment log and trial master file in Google Drive.
  • Manages site protocol deviation tracking and ensures corrective action plans are implemented.
  • Evaluate team environment and implement team building activities.
  • Facilitates visits from sponsors, CROs, RCA and other stakeholders.
  • Initiates and oversees study site purchase order process for supplies and devices.
  • Provides weekly reports to the Clinical Trial Director.
  • Participates in meetings with other supervisors and attends RCA annual National meetings and required training.

Requirements
  • Strong critical thinking and leadership skills
  • 2 years Clinical Research or Regulatory Coordinator experience preferred

Minimum Requirements:
  • High School diploma or the equivalent
  • At least 2 years of clinical research coordinator experience or CRCC Certification/CCRP Certification
  • This position requires a valid California driver's license, a reliable vehicle, and current auto insurance.

Physical Requirements:
  • Must be able to stand for long periods of time
  • Must be able to write
  • Must be able to hold arms at shoulder height
  • Must be able to communicate via telephone
  • Must have manual dexterity to work with ophthalmic equipment

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