A company is looking for a Senior Clinical Research Coordinator to lead all aspects of a patient preference trial in the DC Metro Area.
Key Responsibilities
Manage participant recruitment, retention, and screening for a multi-site study
Ensure compliance with regulatory and institutional policies, including IRB submissions and adverse event monitoring
Oversee data management and quality assurance, including data entry and analysis
Required Qualifications
Associate's degree required; Bachelor's degree may substitute for 2 years of required experience
Minimum of six years of research experience
Experience coordinating a multi-site study preferred
Knowledge of regulatory requirements and research protocols
Must reside in Maryland or the DC Metro Area
Clinical Research Coordinator • Durham, North Carolina, United States