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

Research Executive

Lambda Therapeutic Research
Lambda Therapeutic Research
1+ years
400000 - 700000
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 Executive – Clinical Documentation
Req ID: 1308
Date: January 7, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 400,000 – 700,000


About Lambda Therapeutic Research Ltd.

Lambda Therapeutic Research Ltd. is a 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.

Our mission is to maintain the highest standards of scientific integrity, regulatory compliance, and patient-centric clinical research worldwide.


Role Overview

We are seeking a detail-oriented Research Executive – Clinical Documentation to prepare, review, and ensure the quality of project-related Informed Consent Forms (ICFs) and supportive documents in vernacular languages. The role requires precision, strong linguistic skills, and understanding of medical terminology to ensure accurate and compliant documentation.


Key Responsibilities

  • Prepare project-related Informed Consent Forms (ICFs) and other clinical study documents in vernacular languages, including Gujarati and Hindi.

  • Compare translated and back-translated documents to ensure accuracy and consistency.

  • Ensure all documents are written clearly, using correct grammar, syntax, medical terminology, style, and format as per SOPs and regulatory guidelines.

  • Collaborate with clinical teams to maintain document quality and compliance with study protocols.

  • Assist in ensuring timely delivery of high-quality documentation for clinical studies.


Experience Required

  • Minimum 1 year of experience in clinical documentation, translation, or related roles.

  • Familiarity with clinical research documentation and medical terminology is preferred.


Educational Qualifications

  • Any Graduate with strong command over English and Gujarati languages.


Why Join Lambda Therapeutic Research?

  • Opportunity to work in a global CRO with exposure to clinical study documentation and translation.

  • Develop expertise in clinical documentation, regulatory compliance, and patient-focused communication.

  • Career growth with exposure to diverse clinical trials and mentorship in document management.