Medical Imaging Officer
Company: Lambda Therapeutic Research
Location: Ahmedabad, Gujarat, India
Department: Clinical Trial Operations – Medical Imaging
Job Type: Full-Time
JOB OVERVIEW
The Medical Imaging Officer is responsible for supporting imaging activities in clinical trials by coordinating with investigational sites, radiologists, sponsors, and internal clinical teams. The role involves medical image quality review, site feasibility assessment, Trial Master File (TMF) documentation, imaging data management, compliance with clinical trial protocols, and ensuring timely delivery of imaging-related study activities in accordance with GCP and regulatory guidelines.
KEY RESPONSIBILITIES
Clinical Trial Imaging Operations
Support medical imaging activities for clinical research studies.
Coordinate imaging requirements across clinical trial sites.
Ensure timely collection and processing of imaging data.
Monitor imaging deliverables according to study timelines.
Assist in study start-up and imaging workflow execution.
Medical Imaging Data Management
Review and verify medical imaging data for completeness and quality.
Perform image quality checks in accordance with study protocols.
Track imaging submissions from clinical sites.
Maintain imaging databases and study documentation.
Ensure data accuracy and regulatory compliance.
Site Feasibility & Study Support
Conduct site feasibility assessments for imaging capabilities.
Coordinate with investigators and imaging centers.
Support site onboarding and imaging qualification activities.
Maintain communication with internal and external stakeholders.
Assist with protocol-specific imaging requirements.
Radiologist & Vendor Coordination
Coordinate with radiologists for image interpretation and reporting.
Communicate with imaging vendors and study sites.
Resolve imaging-related queries and documentation issues.
Ensure timely review and reporting of medical images.
Support vendor performance tracking and issue resolution.
Documentation & Compliance
Maintain Trial Master File (TMF) documentation.
Prepare and organize essential study documents.
Ensure compliance with GCP, SOPs, and regulatory requirements.
Maintain audit-ready documentation.
Support internal audits and quality inspections.
Quality Assurance
Perform quality control checks on imaging data.
Verify protocol compliance throughout imaging processes.
Identify discrepancies and support corrective actions.
Maintain high standards of data integrity and documentation quality.
Participate in continuous process improvement initiatives.
EDUCATIONAL QUALIFICATIONS
Required
Bachelor's or Master's Degree in:
B.Sc (Life Sciences)
M.Sc (Life Sciences)
B.Pharm
M.Pharm
Biotechnology
Biochemistry
Microbiology
Clinical Research
Or a related Life Sciences discipline
EXPERIENCE REQUIREMENTS
Required
0–1 year of experience in Clinical Research, Medical Imaging, Clinical Trial Operations, or Healthcare.
Freshers with relevant educational background are encouraged to apply.
Preferred
Exposure to Clinical Trial Operations.
Knowledge of Medical Imaging workflows.
Familiarity with Trial Master File (TMF) documentation.
Understanding of ICH-GCP guidelines and clinical research regulations.
Uttar Pradesh :
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Remote, India | Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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