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Officer - Medical Imaging

Lambda Therapeutic Research
Lambda Therapeutic Research
2+ years
₹3,00,000 – ₹5,00,000 per annum
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Officer – Medical Imaging

Company: Lambda Therapeutic Research Ltd.
Req ID: 1384
Location: Ahmedabad, India
Date Posted: 16 Oct 2025
CTC Range: ₹3,00,000 – ₹5,00,000 per annum


Company Overview

Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India.
With international operations in:

  • Mehsana (India)

  • Las Vegas (USA)

  • Toronto (Canada)

  • Barcelona (Spain)

  • London (UK)

  • Warsaw (Poland)

Lambda delivers end-to-end clinical research services for innovator, biotech, and generic pharmaceutical companies worldwide.


Job Summary

The Officer – Medical Imaging will support clinical trials by reviewing, managing, and ensuring the quality of clinical imaging data across multiple imaging modalities, contributing to high-quality data capture, validation, and study deliverables.


Key Responsibilities

Imaging & Data Management

  • Enter clinical trial data into electronic data collection tools.

  • Conduct quality control (QC) reviews of clinical trial images including:

    • OCT (Optical Coherence Tomography)

    • FFA (Fundus Fluorescein Angiography)

    • CFP (Color Fundus Photography)

    • CT/MRI and other imaging modalities

  • Assist study sites with uploading clinical images following protocol requirements.

  • Train site personnel on image acquisition guidelines.

Data Review & Study Support

  • Perform data review of CRFs, eCRFs, reports, and data listings.

  • Support data analysis activities.

  • Support database lock and study close-out activities, including data reconciliation.

  • Manage and resolve data queries in coordination with study teams.

  • Conduct User Acceptance Testing (UAT) for data collection and transfer systems/tools.

  • Review ongoing clinical/medical aspects of assigned patient data and documents.

Quality & Compliance

  • Ensure audit-ready data quality in alignment with Clinical Compliance and Systems Validation requirements.

  • Contribute to development/review of data capture requirement documents, ensuring alignment with protocol and reporting needs.


Required Experience

  • Minimum 6 months of experience in:

    • Clinical trials, and

    • Optometry

  • Experience in a Central Reading Center (preferred)


Educational Qualifications

  • Bachelor’s or Master’s degree in Optometry,
    OR

  • At least 2 years of professional experience working in clinical optometry