Imaging Endpoints (IE) is a leading Imaging Technology and Clinical Research Organization (iCRO) dedicated to advancing medical imaging to accelerate life-saving treatments. With a vision to “Connect Imaging to the Cure™,” IE plays a pivotal role in oncology clinical trials, supporting groundbreaking drug approvals.
Headquartered in Scottsdale, Arizona, IE has a global presence with offices in Cambridge (USA), London, Leiden, Basel, Hyderabad, and Shanghai. As an affiliate of HonorHealth and Scottsdale Medical Imaging Limited (SMIL/RadPartners), IE is recognized as the world’s largest and most preeminent iCRO in oncology.
Job Description
Imaging Endpoints is seeking a highly organized and detail-oriented Clinical Project Coordinator to support clinical trial operations. This role involves coordinating site evaluations, managing trial documentation, ensuring regulatory compliance, and facilitating communication between sponsors, sites, and internal teams.
Key Responsibilities:
✔ Site Evaluations & Training: Assess clinical trial sites for imaging capabilities and coordinate training sessions.
✔ Trial Master File (TMF) Management: Maintain compliance with SOPs, GCP, and regulatory standards.
✔ Audit Preparation: Ensure study documents are audit-ready and manage discrepancies.
✔ Project Tracking: Monitor study progress, enrollment, and data flow using CRFs and CTIS tasks.
✔ Regulatory Compliance: Adhere to HIPAA, GCP, and protocol guidelines.
✔ Meeting Coordination: Schedule project meetings, document minutes, and generate status reports.
Education & Experience:
- Bachelor’s degree (Life Sciences, Healthcare, or related field preferred).
- 1+ years in clinical trials, healthcare, or medical research (CRC experience is a plus).
- Knowledge of Good Clinical Practice (GCP) and regulatory compliance.
- Proficiency in MS Office, project tracking tools, and clinical databases.
Skills & Competencies:
✅ Strong organizational & time management skills
✅ Attention to detail & problem-solving abilities
✅ Excellent written & verbal communication
✅ Ability to multitask in a fast-paced environment
✅ Self-driven with a proactive approach
Why Join Imaging Endpoints?
- Impactful Work: Contribute to cutting-edge oncology research and life-saving drug development.
- Global Team: Collaborate with experts across North America, Europe, and Asia.
- Career Growth: Opportunities for professional development in clinical research.
- Supportive Culture: IE values integrity, excellence, and teamwork—see our Caring Endpoints initiative here.
Physical Requirements & Travel
- Work Environment: Primarily office-based (remote/hybrid options available).
- Travel: 5-10% (domestic/international) for site visits or meetings.
How to Apply
If you are passionate about clinical research and advancing medical imaging, send your resume to hr@imagingendpoints.com.
Join IE and help Connect Imaging to the Cure™!
