Research Associate

Lambda Therapeutic Research

2-3 years

300000 - 500000

Ahmedabad India

10 Jan. 19, 2026

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

Job Title: Research Associate – Clinical Documentation
Req ID: 1483
Date: January 15, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 300,000 – 500,000

About Lambda Therapeutic Research Ltd.

Lambda Therapeutic Research Ltd. is a leading global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategically located facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), we provide end-to-end clinical research services to global innovators, biotech companies, and pharmaceutical organizations.

We are committed to excellence in clinical research, regulatory compliance, and scientific integrity, enabling our clients to develop safe and effective therapeutics worldwide.

Role Overview

We are seeking a meticulous Research Associate – Clinical Documentation to support the preparation, review, and quality assurance of clinical study documents. The ideal candidate will have experience in clinical documentation, a strong scientific background, and a keen eye for detail to ensure accuracy and regulatory compliance.

Key Responsibilities

Prepare, organize, and maintain high-quality clinical trial documents that accurately reflect study data.
Ensure all deliverables comply with planned timelines, documented guidelines, and standard operating procedures (SOPs).
Assist in supervising, planning, and reviewing a variety of clinical study documents, including:
- Clinical CTD modules
- Investigator brochures
- Clinical trial protocols
- Informed consent forms (ICF)
- Electronic and paper case record forms (CRFs)
- Clinical trial safety reports
- Regulatory submissions
Conduct literature searches, organize information, critically evaluate data, and interpret scientific findings for documentation.
Perform quality checks and reviews of clinical documents to ensure accuracy, consistency, and compliance with regulatory standards.

Experience Required

2–3 years of relevant experience in clinical documentation, regulatory submissions, or clinical research support.

Educational Qualifications

B. Pharm or M. Pharm in Pharmacy or related life sciences discipline.

Why Join Lambda Therapeutic Research?

Work in a global CRO with exposure to international clinical research and regulatory standards.
Hands-on experience in clinical documentation, regulatory submissions, and quality assurance.
Career growth through mentorship, training, and involvement in diverse clinical study projects.

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