Imaging Endpoints (IE), a globally recognized Imaging Clinical Research Organization (iCRO), has announced openings for Clinical Project Coordinator and Clinical Project Coordinator II positions in Hyderabad, Telangana. The company is seeking talented professionals who are passionate about clinical research, medical imaging, and advancing innovative therapies for cancer patients worldwide.
This is an excellent opportunity for candidates interested in clinical project management, clinical research operations, trial coordination, Trial Master File (TMF) management, and Good Clinical Practice (GCP) in a global clinical research environment.
About Imaging Endpoints
Imaging Endpoints is one of the world’s leading imaging contract research organizations specializing in oncology clinical trials. Headquartered in Scottsdale, Arizona, the company has offices across the United States, Europe, China, and India.
The organization supports pharmaceutical and biotechnology companies by providing advanced imaging technologies and services that help accelerate drug development and improve patient outcomes.
Job Details
- Position: Clinical Project Coordinator / Clinical Project Coordinator II
- Company: Imaging Endpoints
- Location: Hyderabad, Telangana, India
- Job Type: Full-Time
- Work Mode: On-site
- Industry: Clinical Research, Medical Imaging, Clinical Trials
- Experience: Freshers and candidates with 1+ years of experience preferred
- Education: Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, Healthcare, or related disciplines
Key Responsibilities
Clinical Trial Site Coordination
- Evaluate site capabilities for imaging clinical trials
- Coordinate and schedule site training activities
- Serve as primary contact for study sites
- Maintain project trackers and study documentation
Trial Master File (TMF) Management
- Maintain and update Trial Master Files
- Ensure documentation compliance with SOPs
- Identify discrepancies and coordinate remediation activities
Clinical Project Management Support
- Assist Project Managers during study startup and execution
- Monitor study enrollment and project milestones
- Generate weekly project and enrollment reports
- Coordinate project meetings and prepare minutes
Clinical Data and Imaging Operations
- Manage Case Report Forms (CRFs) and data queries
- Track imaging scans received via CD or SFTP
- Upload and manage images in PACS repositories
- Support CTIS preprocessing activities
- Perform image reconciliation activities
Audit and Compliance Activities
- Support study audit preparation
- Verify adherence to GCP and SOP requirements
- Maintain regulatory compliance throughout the study lifecycle
- Ensure HIPAA compliance and confidentiality standards
Additional Responsibilities for Clinical Project Coordinator II
- Coordinate system access and site contact management
- Mentor and train new Clinical Project Coordinators
- Lead study closeout activities
- Manage trial communication and reporting activities
Required Qualifications
Educational Requirements
- Bachelor’s Degree in:
- B.Pharm
- Pharm.D
- B.Sc Life Sciences
- Biotechnology
- Microbiology
- Nursing
- Allied Health Sciences
- Other Healthcare or Life Science disciplines
Preferred Experience
- Clinical Research Coordinator (CRC) experience
- Clinical trials industry exposure
- Healthcare operations experience
- Knowledge of Good Clinical Practice (GCP)
- Understanding of Quality Assurance and Compliance processes
Required Skills
Candidates should possess:
- Strong organizational and time management skills
- Excellent written and verbal communication abilities
- Proficiency in Microsoft Office applications
- Attention to detail and multitasking capabilities
- Ability to work independently and collaboratively
- Knowledge of clinical research documentation
- Problem-solving and analytical thinking skills
- Ability to understand technical research protocols
- Strong adaptability and client-focused mindset
Why Join Imaging Endpoints?
Global Clinical Research Exposure
Work with one of the world’s most respected imaging CROs supporting innovative oncology drug development programs.
Career Growth Opportunities
Gain experience in:
- Clinical Project Management
- Clinical Trial Operations
- TMF Management
- Clinical Data Flow Management
- Regulatory Compliance
- Medical Imaging Research
Meaningful Work
Contribute to clinical trials that support the development of potentially life-saving therapies for cancer patients worldwide.
Collaborative Environment
Join a dynamic, global team that values integrity, innovation, accountability, and excellence.
Estimated Salary
Based on comparable Clinical Project Coordinator roles in Hyderabad’s clinical research industry:
- Clinical Project Coordinator: โน4.5 โ โน7 LPA
- Clinical Project Coordinator II: โน7 โ โน10 LPA
Actual compensation may vary depending on qualifications, experience, and company policies.
How to Apply
