Clinical Coordinator

About the job

The Clinical Research Coordinator II/III manages clinical trials from planning through closeout at a CRO in Baltimore, Maryland. The role involves coordinating protocol compliance, mentoring junior staff, and working closely with stakeholders to ensure trial accuracy and quality.

Key Responsibilities

• Oversee study protocol, consent, and documentation.
• Ensure regulatory and GCP compliance in trial conduct.
• Serve as participant point of contact throughout trial phases.
• Collaborate with multidisciplinary teams and sponsors.
• Mentor and assist in training of junior staff.

Qualifications

• Bachelor of Science in a relevant field.
• At least 1 year (CRC II) or 3 years (CRC III) clinical trial coordination experience.
• CRC III requires ACRP/ SOCRA certification.
• Proficiency with GCP, EDC systems, and MS Office.
• Strong organizational and communication skills.

Benefits

• Medical, dental, vision coverage, HRA, FSA.
• Life and disability insurance, 401(k) with employer match.
• Comprehensive employee assistance programs.

Location

• Baltimore, Maryland (On-site only).

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.