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Officer

Lambda Research Accelerated
Lambda Research accelerated
1-4 years
INR 3,00,000 – 5,00,000 per annum
Ahmedabad, India
10 Feb. 18, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Officer – Regulatory Affairs

Job Category: Regulatory Affairs / Clinical Research / CRO

Job Type: Full-Time

Experience Level: 1–4 Years

Location: Ahmedabad, Gujarat, India
Req ID: 1527
CTC Range: INR 3,00,000 – 5,00,000 per annum

Company Overview

Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations across India, North America, and Europe, Lambda provides end-to-end clinical research services to pharmaceutical, biotech, and generic drug companies worldwide. The company specializes in regulatory submissions, clinical operations, and compliance support to accelerate drug development and approval processes.

Role Overview

Lambda Therapeutic Research is seeking a Regulatory Affairs Officer with experience in CDSCO submissions and clinical trial regulatory support. The role will focus on preparing, submitting, and tracking regulatory dossiers for clinical trials and controlled substances, managing electronic trial master files (eTMF), and supporting internal and external audits.

Key Responsibilities

  • EC Submissions: Prepare and file Ethics Committee applications, follow up for approvals, and circulate approvals to relevant stakeholders.

  • eTMF Management: Upload, review, and maintain regulatory documents in the electronic Trial Master File system.

  • Zonal & Central Office Submissions: Prepare dossiers, justification notes, and coordinate approvals for BE-NOC, TL, and CT applications.

  • CBN/NCB Applications: Prepare and submit dossiers for controlled substances; follow up for timely approvals.

  • CTRI Registration: Prepare and submit CTRI applications; coordinate with Clinical Project Managers and track approvals.

  • Query Management: Draft and coordinate responses to regulatory queries; maintain tracker updates.

  • Reporting: Prepare and circulate monthly RA activity reports to management.

  • Audit Support: Assist during system or vendor audits and prepare responses to audit observations.

Required Experience

  • 1–4 years of experience in Regulatory Affairs within a CRO environment.

  • Hands-on exposure to CDSCO submissions, clinical trial regulatory processes, and CTRI registrations.

Technical Skills

  • Knowledge of CDSCO, ICH-GCP, Schedule Y, and CTRI requirements.

  • Proficiency in dossier preparation, eTMF systems, and regulatory trackers.

Soft Skills

  • Strong communication, coordination, and English language proficiency.

  • Attention to detail and ability to manage multiple tasks efficiently.

  • Proactive problem-solving and a collaborative approach to regulatory challenges.

Educational Qualification

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related field.

This position is ideal for regulatory professionals aiming to advance their career in clinical research and regulatory affairs within a global CRO environment.