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Technical Officer - Cdm - Lp

Lambda Therapeutic Research
0-2 years
INR 3.5 LPA – 7 LPA
Ahmedabad, India
1 July 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Technical Officer – Clinical Data Management (CDM) – Late Phase

Company: Lambda Therapeutic Research Ltd.
Location: Ahmedabad, Gujarat, India
Department: Clinical Data Management (CDM) – Late Phase
Job Type: Full-Time
Experience: Clinical Data Management


JOB OVERVIEW

The Technical Officer – Clinical Data Management (CDM) is responsible for supporting late-phase clinical trials through eCRF design, clinical data validation, query management, medical coding, external data reconciliation, and clinical database management. The role involves participating in study start-up, conduct, and close-out activities while ensuring high-quality, regulatory-compliant clinical data in accordance with GCP, CDISC standards, and applicable SOPs.


KEY RESPONSIBILITIES

Clinical Data Management

  • Manage clinical trial data.

  • Support late-phase clinical studies.

  • Maintain clinical databases.

  • Ensure data quality and integrity.

  • Perform database reviews.

  • Support database lock activities.

  • Participate in study close-out.

eCRF Development

  • Design electronic Case Report Forms (eCRFs).

  • Develop eCRF specifications.

  • Test eCRFs.

  • Validate eCRF functionality.

  • Conduct User Acceptance Testing (UAT).

  • Deliver eCRF training.

  • Support database deployment.

Data Validation

  • Perform clinical data validation.

  • Execute edit checks.

  • Identify data discrepancies.

  • Validate clinical datasets.

  • Ensure data consistency.

  • Perform quality checks.

  • Review clinical data for completeness.

Query Management

  • Generate data queries.

  • Review investigator responses.

  • Resolve clinical queries.

  • Track outstanding queries.

  • Ensure timely query resolution.

  • Maintain query documentation.

Medical Coding

  • Perform medical coding.

  • Code adverse events.

  • Code medical history.

  • Code concomitant medications.

  • Utilize MedDRA.

  • Utilize WHO Drug Dictionary (WHO-DD).

  • Ensure coding accuracy.

Data Reconciliation

  • Perform external data reconciliation.

  • Reconcile laboratory data.

  • Review vendor data.

  • Validate external datasets.

  • Resolve reconciliation discrepancies.

  • Document reconciliation activities.

Clinical Study Support

  • Participate in study start-up.

  • Support study conduct.

  • Assist during study close-out.

  • Attend project meetings.

  • Coordinate with cross-functional teams.

  • Support project timelines.

Documentation & Compliance

  • Prepare CDM documentation.

  • Maintain study documentation.

  • Follow SOPs.

  • Ensure GCP compliance.

  • Maintain audit-ready documentation.

  • Support inspection readiness.

Training & Collaboration

  • Conduct eCRF training sessions.

  • Collaborate with Clinical Operations.

  • Coordinate with Data Management teams.

  • Work with Biostatistics and Programming teams.

  • Support sponsor communications.


EDUCATIONAL QUALIFICATIONS

Required

  • M.Pharm

  • M.Sc. (Life Sciences)

  • BHMS

  • BAMS

  • BDS