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Full Time Clinical Research Rater Jobs in California

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Full Time Clinical Research Rater information

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 key skills and qualifications needed to thrive as a Full Time Clinical Research Rater, and why are they important?

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 Full Time Clinical Research Raters?

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 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 July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Full Time Clinical Research Coordinator Exp. w/ Drug Studies

Allergy and Asthma Associates of Southern California

Laguna Niguel, CA

$24 - $28/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 15 days ago

Job description

Full Time Clinical Research Coordinator Exp. w/ Drug Studies

Allergy & Asthma Associates of Southern California dba. Southern California Research

28202 Cabot Road, Laguna Niguel, CA 92677

Job details

Pay: $24 - $28 an hour

Job type: Full-time

Shift and schedule

  • 8-hour shift
  • Monday to Friday

Expected hours: 40 per week

Experience: Clinical Research Coordinator: 1 year (Required)

Work Location: In person

Benefits

  • 401(k)
  • Health insurance
  • Paid time off
  • Vision insurance
  • Dental insurance

Full job description

Must have clinical drug study experience. We are a fast-paced research center currently looking to add an experienced research coordinator to our staff. Ideal candidates will possess the following qualifications:

  • Experience as a clinical research coordinator
  • Ability to work as a team member
  • Self -starter and ability to work independently
  • Excellent communication skills, written and verbal
  • Organized and attention to detail, ability to work in a fast-paced environment
  • Ability to adapt to changing schedules
  • Supply and inventory management
  • Third party vendor management
  • Facilitate monitoring visits (IMVs) and sponsor correspondence including managing the follow-up process
  • IP management, dispensation, and accountability
  • Adverse Event management, tracking, reporting, and follow-up
  • Able to review study protocols, create source documents, maintain regulatory binders
  • Conduct patient recruitment and enrollment of eligible patients
  • Experience consenting, screening and randomizing subjects
  • Ability to multitask, prioritize and identify urgent matters
  • Able to obtain vital signs, ECG’s, give injections
  • Phlebotomy certified, IATA certified and experience processing labs
  • Computer skills—including used of Microsoft Office Suite
  • CCRC or working towards obtaining certification. GCP Certification is required at the very least
  • Understands GCP, ICH and FDA guidelines and requirements
  • This role is 100% onsite. Candidates must be willing to relocate before starting work if not already located in the area.