Clinical Research Coordinator

Benefits

Qualifications

• •2+ years of experience as a Clinical Research Coordinator in a site setting
• •Strong understanding of GCP, ICH guidelines, and clinical research regulations
• •Experience with EDC systems and CTMS platforms
• •Excellent organizational skills with the ability to manage multiple protocols simultaneously
• •Strong interpersonal and communication skills, with a patient-centered approach
• •Ability to work fully on-site in Pleasanton, CA
• •3 more items(s)

Responsibilities

• •This is a fully on-site role ideal for someone who thrives in a fast-paced environment and enjoys working closely with patients, investigators, and cross-functional teams
• •Coordinate and manage day-to-day activities for multiple clinical trials from start-up through close-out
• •Screen, recruit, and consent study participants in accordance with protocol requirements
• •Schedule and conduct study visits, ensuring protocol adherence and participant safety
• •Collect, enter, and maintain accurate study data in EDC systems and source documents
• •Prepare for and support monitoring visits, audits, and regulatory inspections
• •Maintain regulatory binders and ensure compliance with GCP, FDA, and IRB requirements
• •Process and ship laboratory specimens per protocol guidelines
• •Collaborate closely with investigators, sponsors, and internal teams to ensure study success
• •Track study timelines, enrollment metrics, and report on progress as needed
• •7 more items(s)