Senior Clinical Research Coordinator Job at Sunwise Clinical Research, LLC, Walnut Creek, CA

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  • Sunwise Clinical Research, LLC
  • Walnut Creek, CA

Job Description

Job Description

Senior Clinical Research Coordinator

We are seeking an experienced and detail-oriented Senior Clinical Research Coordinator to manage the operational aspects of industry-sponsored clinical trials. This role requires at least 2–5 years of experience coordinating clinical trials, with a strong understanding of protocol adherence, regulatory compliance, and sponsor interactions.

Key Responsibilities:

  • Coordinate day-to-day activities of assigned clinical trials from startup to closeout
  • Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements
  • Prepare and maintain regulatory documents, including IRB submissions and essential files
  • Coordinate study visits, scheduling, and study assessments in collaboration with clinical staff
  • Accurately document procedures and maintain EDC systems and source documents
  • Serve as a primary point of contact for monitors, sponsors, and study teams
  • Assist with budget tracking, invoicing, and sponsor correspondence
  • Support the development and training of junior research staff

Qualifications:

  • Bachelor’s degree in a health-related field or equivalent experience
  • Minimum 2–5 years of experience coordinating industry-sponsored clinical trials
  • Must be familiar with working on multiple studies at once
  • Strong working knowledge of FDA regulations, ICH-GCP, and clinical research workflows
  • Excellent organizational, communication, and documentation skills
  • Clinical research certification (ACRP or SOCRA) preferred but not required

(35$ - 40$)/HR

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