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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