Clinical Research Coordinator I

Responsibilities

• Act as lead coordinator on clinical studies and execute follow-up visits
• Perform daily tasks including document review, data entry, and test material preparation
• Conduct study setup in compliance with protocol, SOPs, and GCP guidelines
• Manage study documentation including protocol amendments, case report forms, and EDC
• Coordinate subject scheduling and monitor panelist compliance
• Respond to queries from Quality Assurance and Statistics departments
• Ensure staff understand and perform duties according to protocol and SOPs

Requirements

• Associate degree or minimum 2 years of relevant work experience with a GED/High School Diploma
• Basic understanding of clinical research concepts
• Ability to manage multiple projects in a fast-paced environment
• Strong mathematical, reasoning, and computer skills

Benefits

• Medical, dental, and vision insurance
• 401(k) with company match and immediate vesting
• Annual bonus target and employee referral program
• Professional growth through online training and tuition reimbursement
• Paid time off including vacation, sick, holidays, and volunteer time

About the Company

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