Clinical Coordinator

About the job

This position coordinates clinical research activities from planning to study completion, ensuring regulatory compliance, data integrity, and patient care in a CRO environment. You'll work across multiple therapeutic areas, collaborating with internal departments to support trials.

Key Responsibilities

• Coordinate clinical trial phases and ensure compliance with GCP and SOPs
• Review study protocols, patient consent, and study documents
• Serve as a liaison between clinicians, pharmacy, lab, and regulatory affairs
• Conduct participant screening, eligibility assessment, and direct participant support
• Maintain accurate study records, documentation, and logs
• Prepare for study monitoring visits and assist with product preparation

Qualifications

• Associate degree with clinical research experience or relevant background
• Familiarity with GCP/Code of Federal Regulations
• Strong time management and detailed documentation skills

Benefits

• Employer-paid health, dental, vision insurance
• 401(k) with employer match
• Paid life and disability insurance
• Flexible Spending Accounts and Employee Assistance Program

Location

• Baltimore, MD

Culture

• Collaborative environment emphasizing teamwork, innovation, and employee well-being
• Equal opportunity and inclusion focused

Healthcare · 10,000+

Pharmaron is a premier life science service provider offering comprehensive research, development, and manufacturing capabilities throughout the drug discovery, preclinical, clinical development, and commercialization process. Founded in 2004 and headquartered in Beijing, China, the company operates globally with over 21,000 employees across China, the U.S., and the U.K. Pharmaron specializes in small molecules, biologics, and cell and gene therapy products, delivering integrated solutions to partners worldwide.