Sunwise Clinical Research, LLC
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