Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Technical Officer - Cdm - Lp

Lambda Research accelerated
0-2 years
INR 3 LPA – 6 LPA
Ahmedabad, India
1 June 11, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology

Technical Officer – CDM (Late Phase)

Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, Gujarat
Req ID: 1588
Employment Type: Full-Time
Department: Clinical Data Management (CDM) – Late Phase
CTC Offered: ₹3.5 – ₹7 LPA

About the Role

Lambda Therapeutic Research is hiring a Technical Officer – CDM (Late Phase) to support Clinical Data Management activities across Late Phase Clinical Trials. The role involves eCRF design, data validation, query management, medical coding, external data reconciliation, and study support throughout the project lifecycle from startup to close-out.

Key Responsibilities

eCRF Development & Study Setup

  • Design and develop eCRFs for Late Phase clinical studies.

  • Perform eCRF testing and validation activities.

  • Support database build and study startup activities.

  • Ensure eCRFs align with protocol and study requirements.

Data Validation & Query Management

  • Perform ongoing clinical data review and validation.

  • Generate, track, and resolve data queries.

  • Ensure timely resolution of discrepancies.

  • Maintain data quality and database integrity throughout the study.

Medical Coding

  • Perform coding of:

    • Adverse Events (AEs)

    • Medical History

    • Concomitant Medications

  • Utilize standard coding dictionaries such as MedDRA and WHO Drug.

External Data Reconciliation

  • Reconcile external data sources with clinical databases.

  • Review laboratory, safety, and vendor data.

  • Identify and resolve data inconsistencies.

Study Conduct & Close-Out Support

  • Participate in project startup, conduct, and close-out activities.

  • Attend project meetings and provide CDM updates.

  • Support database lock activities and final data review.

  • Ensure study documentation is complete and audit-ready.

Training & Documentation

  • Conduct eCRF and database training sessions.

  • Prepare and maintain:

    • CDM Documentation

    • Validation Documentation

    • Query Management Logs

    • Reconciliation Reports

  • Ensure compliance with SOPs and regulatory requirements.

Key Deliverables

  • eCRF Development & Testing

  • Data Validation Outputs

  • Query Management Activities

  • Medical Coding Deliverables

  • External Data Reconciliation Reports

  • Clinical Data Management Documentation

  • Study Training Records

Required Qualifications

Education:

  • M.Pharm

  • BAMS

  • BHMS

  • BDS

  • M.Sc. (Life Sciences)

Required Skills

  • Clinical Data Management (CDM)

  • eCRF Design & Development

  • Database Testing

  • Data Validation

  • Query Management

  • Medical Coding

  • MedDRA

  • WHO Drug Coding

  • Data Reconciliation

  • Clinical Research

  • Database Lock Activities

  • EDC Systems

  • Clinical Trial Documentation

  • SOP Compliance

Preferred Candidate Profile

  • Experience in Clinical Data M