Clinical Project Coordinator at Imaging Endpoints | Clinical Data Management & Life Science Jobs
Join Imaging Endpoints, a global imaging clinical research organization, as a Clinical Project Coordinator. This exciting opportunity lets you play a key role in clinical data management and project coordination within groundbreaking oncology trials. Be part of a passionate team that’s redefining how imaging connects to the cure, advancing your career in life science jobs that truly make an impact.
About the Company:
Imaging Endpoints (IE) is a leading Imaging Technology and Imaging Clinical Research Organization (iCRO) dedicated to connecting imaging to the cure™. Headquartered in Scottsdale, Arizona, with offices across the US, UK, Europe, China, and India (Hyderabad), IE partners with global leaders to deliver cutting-edge solutions in clinical research. As the world’s largest iCRO in oncology, IE is an affiliate of HonorHealth and Scottsdale Medical Imaging Limited (RadPartners), committed to excellence, ethics, and innovation in advancing medical breakthroughs.
Job Overview:
Under the direction of Imaging Operations Management, the Clinical Project Coordinator will support operations, sponsors, and study sites to ensure seamless coordination of clinical project activities. This role bridges technology and science to ensure compliant, efficient clinical data management and support for oncology trials
worldwide.- Location: Hyderabad, India
- Job Type: Full-Time
Qualifications:
- Bachelor’s degree required (Life Sciences preferred)
- 0–2 years of experience in the clinical research or healthcare industry
- Prior experience as a Clinical Research Coordinator (CRC) preferred
- Familiarity with GCP and Quality Assurance/Compliance standards
- Strong organizational, analytical, and time management skills
- Proficiency in Microsoft Office and internet-based tools
Key Responsibilities:
- Evaluate clinical trial sites following SOPs and report findings to Project Managers.
- Manage and maintain the Trial Master File (TMF) to ensure completeness and compliance.
- Support clinical data management tasks, including data tracking, query resolution, and CRF management.
- Assist in audit preparation, document verification, and process compliance.
- Coordinate site training sessions and maintain project trackers and enrollment updates.
- Collaborate with teams for image uploads, reconciliations, and project lifecycle management.
- Generate and maintain weekly status reports and site communications.
- Train and mentor new coordinators as needed.
- Maintain confidentiality and adhere to HIPAA and regulatory guidelines.
Skills Required:
- Strong understanding of clinical data management principles
- Proficiency in MS Office and electronic trial systems
- Excellent verbal and written communication skills
- Detail-oriented, proactive, and adaptable to project needs
- Strong interpersonal and teamwork abilities
- Ability to multitask, prioritize, and meet deadlines
- Commitment to high-quality standards in clinical research
At Imaging Endpoints, your work in clinical data management contributes directly to improving lives through better cancer treatments and medical imaging advancements. If you’re passionate about life science jobs that create real-world impact, this is your chance to grow with a visionary global leader.
How to Apply:
Visit the Imaging Endpoints careers page for more details and to submit your application.
