Imaging Endpoints, a global Imaging Clinical Research Organization (iCRO), is hiring a Clinical Project Coordinator / Clinical Project Coordinator II for its Hyderabad office. This is an excellent opportunity for life science graduates and clinical research professionals seeking to build a career in imaging-based clinical trials, oncology research, and project coordination.
Imaging Endpoints is recognized as the world’s largest and most preeminent imaging CRO in oncology, supporting multiple global drug approvals and innovative clinical trials. Candidates with experience as Clinical Research Coordinator (CRC), TMF Specialist, or clinical operations staff will be highly preferred.
🏢 Company Overview – Imaging Endpoints
Imaging Endpoints (IE) is an imaging technology and imaging CRO headquartered in Scottsdale, Arizona, with offices across the USA, Europe, and Asia, including Hyderabad, India. IE focuses on connecting imaging to the cure by advancing imaging science and supporting oncology clinical trials worldwide.
💼 Job Title
- Clinical Project Coordinator
- Clinical Project Coordinator II
📍 Job Location
Hyderabad, Telangana, India (On-site)
📝 Key Responsibilities
- Conduct site evaluations for imaging capability in assigned clinical trials
- Coordinate and schedule site trainings
- Act as primary contact for clinical trial sites
- Maintain and own Trial Master File (TMF)
- Ensure audit readiness and compliance with SOPs and GCP
- Support Project Manager (PM) during study start-up and lifecycle
- Track scans via CD or 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 protocol, regulatory, and HIPAA requirements
🎓 Qualifications & Experience
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- Minimum 0–1 year (CPC) or 1+ year (CPC II) experience in medical or clinical trials industry
- Prior experience as Clinical Research Coordinator (CRC) preferred
- Knowledge of GCP and clinical trial compliance
- Proficiency in MS Office and internet applications
- Strong organizational, communication, and multitasking skills
🧠 Required Skills
- Attention to detail
- Time management and organization
- Ability to work independently and in teams
- Understanding of technical research protocols
- Service-oriented and proactive attitude
🎁 Benefits
- Competitive salary package
- Global exposure in oncology imaging trials
- Career growth and training opportunities
- Work with a leading imaging CRO
- Supportive and collaborative work environment
📤 How to Apply
📅 Application Details
