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Clinical Research Rater Jobs in California (NOW HIRING)

Tekberry

Clinical Research Coordinator

Stanford, CA · On-site

$44 - $51/hr

Clinical Research Coordinator Pay Rate Range: $44.00 - $51.00/hr. (W2) (DOE) Employment Type: Contract (Potential Temp-to-Hire) Duration: Approximately 6 Months (Potential Extension/Conversion ...

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

Clinical Research Specialist Hybrid - onsite every Monday, Wednesday, and every other Friday Pay Rate: 92,000Clinical Research Specialist RequisitionJob Overview This Clinical Research Specialist ...

Tekberry

Clinical Research Coordinator

Palo Alto, CA · On-site

$35 - $70/hr

Clinical Research Coordinator Pay Rate Range: $35.00 - $70.00/hr (DOE, based on experience and level) Employment Type: Contract Schedule: Full-time, Monday - Friday | 8:00 AM - 5:00 PM Location:

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How much do clinical research rater jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for clinical research rater in California is $22.41, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $25.62 per hour, depending on experience, location, and employer.

What is a clinical research rater?

A Clinical Research Rater is responsible for administering standardized assessments and interviews to clinical trial participants to evaluate their cognitive, psychiatric, or neurological status. They work closely with investigators and study coordinators to ensure data accuracy and consistency in clinical trials. Raters must be trained in administering rating scales and maintaining objectivity in their evaluations. This role is critical in ensuring the integrity of clinical trial outcomes, especially in studies related to mental health, neurology, and other therapeutic areas.

What are the key skills and qualifications needed to thrive in the clinical research rater position?

To thrive as a Clinical Research Rater, you need a background in psychology, neuroscience, or a related health science field, with strong attention to detail and standardized assessment skills. Familiarity with clinical trial protocols, electronic data capture systems, and rating scales like the Hamilton Depression Rating Scale or PANSS is often required. Excellent observational, interpersonal, and communication skills help you accurately assess participants and collaborate with multidisciplinary research teams. These abilities ensure precise data collection and reporting, which are critical for the validity and success of clinical research studies.

What are some typical challenges faced by clinical research raters in their daily work?

Clinical Research Raters often face the challenge of maintaining objectivity and consistency while administering complex assessments across diverse participant populations. They must carefully follow study protocols, manage detailed documentation, and adapt to changes in trial requirements or participant schedules. Working closely with other research staff and clinicians requires strong communication and teamwork, especially when addressing discrepancies or unexpected findings. Staying up to date with assessment tools and best practices helps minimize errors and supports the integrity of the study data.

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 Clinical Research Rater jobs in California?

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

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

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

Clinical Research Rater jobs near you
Infographic showing various Clinical Research Rater job openings in California as of August 2026, with employment types broken down into 78% Full Time, and 22% Part Time. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $46,622 per year, or $22.4 per hour.

Clinical Research Coordinator (Experienced) - Westside Los Angeles

Irvine Clinical Research

Los Angeles, CA

$62K - $83K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 13 days ago

Job description

Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
 
We are seeking a dedicated and experienced Clinical Research Coordinator to drive trial success at our Oakland location. This role is ideal for a seasoned CRC (internally leveled as a CRC II, III, or IV depending on experience) who is ready to take ownership of complex Phase II and III clinical trials. You will work closely with our Principal Investigators and clinical team to ensure the highest standards of data integrity, patient safety, and operational excellence.
Job Duties

  • Study Management: Serve as the primary or co-coordinator for assigned Phase II/III clinical research studies, overseeing day-to-day operations from site initiation to closeout.

  • Protocol Compliance: Execute study procedures with strict adherence to Good Clinical Practice (GCP) guidelines, FDA regulations, and specific study protocols.

  • Patient Coordination: Guide participants through complex visit schedules, including consenting, screening, and coordinating cross-functional appointments (e.g., imaging, infusions).

  • Data Integrity: Timely and accurately enter, organize, and maintain study data across various electronic platforms (eSource, EDC, CTMS), proactively resolving queries.

  • Clinical Assessments: Conduct vital signs, ECGs, and other protocol-specific diagnostic, efficacy, and safety assessments.

  • Quality & Audit Readiness: Maintain impeccable regulatory and source documentation, ensuring the site is consistently prepared for sponsor monitoring visits and audits.

Job Requirements

  • Experience: 2 to 4+ years of hands-on experience coordinating industry-sponsored clinical trials (prior experience in CNS, Neurology, or Psychiatry is a strong plus).

  • Technical Skills: Demonstrated ability to navigate complex clinical trial management systems (CRIO eSource & CTMS) and EDC platforms quickly and accurately.

  • Organization & Precision: Exceptional attention to detail, capable of managing competing priorities and complex visit windows without compromising quality.

  • Communication: A strong, professional command of spoken and written English, with a proven ability to build rapport with older adult populations and their study partners.

$62,400 - $83,200 a year
Hours and Compensation
  • Location: This is a full-time employment position based in-person at our Inglewood Clinical / Westside Los Angeles site in Ladera Heights: 5120 W Goldleaf Cir, Ste 250, Los Angeles, CA 90056

  • Compensation: The expected salary range for this position is $30-40 per hour ($62,400 to $83,200 per year). Final compensation offers will be determined based on the candidate's specific internal level (CRC II - IV), years of relevant clinical trial experience, and applicable clinical certifications (e.g., CCRC, nursing, or phlebotomy license).

  • Insurance: The company pays for 100% of health, dental, and vision individual insurance costs for eligible full-time employees.

  • Paid Time Off: Vacation (PTO) is earned at a rate of 3 weeks per year.

Equal Opportunity & Fair Chance Employer Irvine Clinical Research and its affiliates are Equal Opportunity Employers. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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