Clinical Data Coordinator Job For BSc Life Sciences at Imaging Endpoints, Apply at Biotecnika
Job Role: Clinical Data Coordinator
Company: Imaging Endpoints
Location: Hyderabad, Telangana
Department: Clinical Data Management
Experience: Minimum 1 year in clinical data management
Position Summary:
Imaging Endpoints is seeking a dedicated and detail-oriented Clinical Data Coordinator II
to support clinical trial data management activities, focusing on imaging data processing, data review, quality control, and system validation. This role ensures accuracy, compliance, and timely delivery of high-quality datasets for analysis and reporting in support of global clinical research studies.
Key Responsibilities:
• Process radiological images in compliance with project-specific protocols and SOPs.
• Enter clinical trial data into electronic and paper-based data collection tools.
• Perform quality control reviews of CRFs, eCRFs, reports, and data listings.
• Generate, track, and resolve data queries related to images and clinical
documentation.
• Support data and image transfers in accordance with timelines and standards.
• Monitor radiology reader activities during on-site or remote assessments.
• Track progress of Data Entry (DE) and Quality Control (QC) activities.
• Generate and quality control Diagnostic and Summary Reports.
• Assist with data analysis, database lock preparation, and study closeout tasks.
• Conduct user
• Maintain accurate project documentation and files (electronic and paper).
• Contribute to the development of Study Specific Procedures (SSPs) and data tools.
• Support Clinical Data Managers and mentor junior staff as needed.
• Provide regular updates to project teams and leadership on task status and
deliverables.
• Ensure high-quality work is completed on time for internal and external stakeholders.
• Perform additional tasks as assigned to support project or departmental goals.
Education & Experience:
• Bachelor’s Degree (Life Sciences or related field preferred)
• Minimum 1 year of clinical data management experience required
• Familiarity with electronic data capture (EDC) systems
• Intermediate knowledge of SAS or similar analysis software preferred
• Understanding of Good Clinical Practices (GCP) and medical terminology
• Knowledge of clinical research or healthcare industry workflows
Key Skills:
• High attention to detail and analytical thinking
• Strong verbal and written communication skills
• Ability to multitask and meet deadlines under pressure
• Excellent organizational and time management abilities
• Collaborative, professional, and proactive work style
• Confidentiality and compliance-focused
• Quick learner, adaptable to new tools and systems
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