Clinical Project Coordinator

Roles & Responsibilities
• Conduct site evaluations for imaging capabilities in assigned clinical trials
• Coordinate and schedule site trainings and act as primary site contact
• Maintain and manage Trial Master File (TMF) ensuring audit readiness
• Support Project Manager during study start-up and ongoing trial activities
• Track imaging scans via CD/SFTP and upload into PACS-RAW repository
• Manage CRFs, queries, and clinical data flow
• Generate weekly project, site, and enrollment reports
• Schedule meetings, prepare agendas, and document minutes
• Perform User Acceptance Testing (UAT) and image reconciliation
• Ensure compliance with SOPs, GCP, protocol, regulatory, and HIPAA requirements

Qualification
• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field

Experience
• CPC: 0–1 year experience in clinical trials or medical research
• CPC II: 1+ year experience in clinical trials or imaging studies
• Prior experience as Clinical Research Coordinator (CRC) preferred

Skills
• Strong knowledge of GCP and clinical trial processes
• Excellent organizational, communication, and multitasking skills
• Proficiency in MS Office and internet-based applications
• High attention to detail and ability to work independently and in teams

About the Organization
Imaging Endpoints is the world’s leading imaging Clinical Research Organization (iCRO), specializing in oncology and imaging-based clinical trials. The company supports global drug development programs through innovative imaging solutions and high-quality clinical trial execution.