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Assistant Clinical Research Rater Jobs in California

CenExel

Medical Assistant - Clinical Research

Anaheim, CA · On-site

$20 - $21/hr

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Medical Assistant Certification or Certified Phlebotomy Tech or (Required) * Medical Assistant ...

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Assistant Clinical Research Rater information

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 California? The most popular types of Clinical Research Rater jobs in California are:
What cities in California are hiring for Assistant Clinical Research Rater jobs? Cities in California with the most Assistant Clinical Research Rater job openings:
Assistant Clinical Research Rater jobs near you
Assistant Clinical Research Coordinator

Assistant Clinical Research Coordinator

Avispa Technology

Palo Alto, CA • On-site

$34/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Job Description
Assistant Clinical Research Coordinator 1503779
  • Hourly pay: $34/hr
  • Worksite: Leading university (Palo Alto, CA 94304 - Hybrid)
  • W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
  • 40 hours/week, 5 Month Assignment (With possibility of extension)

A leading university is seeking an Assistant Clinical Research Coordinator to support the coordination and execution of clinical research studies. This role assists with participant recruitment, data collection, regulatory documentation, and study operations while ensuring compliance with research protocols and regulatory requirements.
Assistant Clinical Research Coordinator Responsibilities:
  • Coordinate study activities by scheduling participant visits, assisting with recruitment, screening, informed consent, follow-up communications, and processing study compensation upon completion.
  • Collect, review, and maintain accurate clinical research data by administering study questionnaires, extracting information from medical records, completing case report forms, and ensuring data quality and completeness.
  • Prepare and maintain regulatory and study documentation, including consent forms, subject logs, correspondence, and other research records in compliance with study protocols and regulatory requirements.
  • Support clinical research procedures by collecting and processing study specimens, performing basic patient measurements and tests (such as vital signs, phlebotomy, and EKG after appropriate training/certification), and preparing specimens for shipment.
  • Maintain study operations by ordering supplies, managing research equipment, collaborating with the study team, and supporting additional study activities as assigned.

Assistant Clinical Research Coordinator Qualifications:
  • 1 year of clinical research or related experience.
  • Experience with clinical research data entry and electronic medical records (EPIC is preferred).
  • General knowledge of medical terminology.
  • Ability to maintain accurate research documentation and regulatory records with strong organizational, communication, and attention-to-detail skills.
  • Working toward certification to perform basic patient procedures, such as phlebotomy and EKG, is preferred.
  • Valid California Class C Driver's License.

Shift:
  • Hybrid: 3-4 days onsite per week.

(H)

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