Clinical Research Coordinator II

Responsibilities

• Coordinate and facilitate daily clinical study activities according to protocol, GCP, SOP, and regulations
• Set up and conduct studies in compliance with protocol and applicable regulations
• Prepare and maintain study documentation including protocol amendments, case report forms, and EDC
• Perform station and instrumentation duties including collection and recording of clinical information
• Ensure staff perform duties according to protocol, SOPs, and GCPs
• Assist in training and mentoring new clinic staff
• Conduct pre-study meetings and review draft protocols and recruiting materials

Requirements

• Bachelor's degree in science or equivalent
• Understanding of basic clinical research concepts
• 2+ years of relevant work experience or equivalent combination of education and experience

Preferred Qualifications

• CCRC/CCRA certification

About the Company

SGS is the world's leading testing, inspection and certification company, recognized as the global benchmark for sustainability, quality and integrity.