Imaging Endpoints (IE) is a globally recognized Imaging Technology and Imaging Clinical Research Organization (iCRO) dedicated to advancing imaging science, technology, and services to bring curative technologies to humankind. With a vision to Connect Imaging to the Cure™, IE has played a pivotal role in supporting some of the most impactful new drug approvals in oncology.
Headquartered in Scottsdale, Arizona, IE has a global presence with offices in Cambridge (USA), London (UK), Leiden (Netherlands), Basel (Switzerland), Hyderabad (India), and Shanghai (China). 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.
IE’s team is passionate about improving the lives of cancer patients through innovative imaging solutions. The company fosters a collaborative, ethical, and excellence-driven work environment, making it a rewarding place to grow your career.
Job Description: Clinical Data Coordinator
Imaging Endpoints is seeking a Clinical Data Coordinator to join its dynamic team in Hyderabad. This role is ideal for individuals with a strong background in clinical data management and a passion for contributing to groundbreaking clinical trials.
Key Responsibilities:
- Process radiological images and clinical trial data in compliance with standard operating procedures (SOPs).
- Enter and review clinical trial data in electronic data capture (EDC) systems.
- Conduct quality control (QC) reviews of case report forms (CRFs), electronic CRFs (eCRFs), and reports.
- Generate, track, and resolve data queries related to images, CRFs, and eCRFs.
- Monitor radiology readers and ensure timely on-site reads.
- Support database lock, study closeout, and reconciliation activities.
- Perform User Acceptance Testing (UAT) for data collection and transfer tools.
- Maintain accurate project files (both paper and electronic) in accordance with SOPs.
- Collaborate with Clinical Data Managers and contribute to the development of study-specific procedures (SSPs) and reports.
- Assist in training and monitoring junior team members.
- Communicate project statuses and deliverables effectively to internal and external stakeholders.
Education and Experience:
- Bachelor’s degree or equivalent combination of education and work experience.
- Minimum 1 year of experience in clinical data management.
- Intermediate knowledge of analysis software (e.g., SAS) is preferred.
- Familiarity with electronic data capture (EDC) systems and Good Clinical Practices (GCP).
- Working knowledge of medical terminology and the clinical trials/healthcare industry.
- Proficiency in MS Office and internet applications.
Skills and Competencies:
- Exceptional attention to detail and strong written/verbal communication skills.
- Ability to multitask, prioritize, and work under pressure in a team environment.
- Strong organizational and time management skills.
- Self-motivated with the ability to grasp new concepts quickly.
- High ethical standards and commitment to maintaining confidentiality.
Why Join Imaging Endpoints?
- Passion-Driven Work: Be part of a team that is dedicated to improving the lives of cancer patients through innovative imaging solutions.
- Global Impact: Contribute to groundbreaking clinical trials that have led to significant drug approvals in oncology.
- Collaborative Environment: Work with a diverse, talented, and supportive global team.
- Career Growth: Opportunities for professional development and advancement in a rapidly growing organization.
- Work-Life Balance: Hybrid work model offering flexibility and a supportive workplace culture.
