Sunwise Clinical Research, LLC
Senior Clinical Research Coordinator
Sunwise Clinical Research, LLC, Walnut Creek, California, United States, 94598
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.
Make your application after reading the following skill and qualification requirements for this position.
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$)/HR
Senior Clinical Research Coordinator
to manage the operational aspects of industry-sponsored clinical trials. This role requires at least 2–5 years of experience coordinating clinical trials, with a strong understanding of protocol adherence, regulatory compliance, and sponsor interactions.
Make your application after reading the following skill and qualification requirements for this position.
Key Responsibilities: Coordinate day-to-day activities of assigned clinical trials from startup to closeout Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements Prepare and maintain regulatory documents, including IRB submissions and essential files Coordinate study visits, scheduling, and study assessments in collaboration with clinical staff Accurately document procedures and maintain EDC systems and source documents Serve as a primary point of contact for monitors, sponsors, and study teams Assist with budget tracking, invoicing, and sponsor correspondence Support the development and training of junior research staff
Qualifications: Bachelor’s degree in a health-related field or equivalent experience Minimum 2–5 years of experience coordinating industry-sponsored clinical trials Must be familiar with working on multiple studies at once Strong working knowledge of FDA regulations, ICH-GCP, and clinical research workflows Excellent organizational, communication, and documentation skills Clinical research certification (ACRP or SOCRA) preferred but not required
(35$ - 40$)/HR