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Research Executive

Lambda Research Accelerated
Lambda Research accelerated
1+ years
400000 - 700000
10 Jan. 12, 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
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 400,000 – 700,000

Organizational Overview:
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 the global innovator, biotech, and generic pharmaceutical industries.

Position Overview:
We are seeking a detail-oriented Research Executive to support clinical trial documentation, including preparation and review of Informed Consent Forms (ICF) and other study-related documents in vernacular languages. This role requires proficiency in English and Gujarati, strong attention to detail, and familiarity with clinical documentation standards and regulatory guidelines.

Key Responsibilities:

  • Prepare project-related Informed Consent Forms (ICF) and other supporting clinical trial documents in Gujarati and Hindi languages.

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

  • Ensure documents are written clearly with correct grammar, syntax, medical terminology, and style, following SOPs and regulatory guidelines.

  • Maintain high-quality standards in clinical documentation to support study compliance.

  • Collaborate with clinical teams to ensure timely preparation and delivery of documents.

  • Perform additional tasks as assigned to support study operations.

Experience Required:

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

Educational Qualification:

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

Why Join Lambda Therapeutic Research:

  • Work with a global CRO operating across multiple countries.

  • Gain exposure to clinical trial documentation and regulatory compliance processes.

  • Opportunities for professional growth and skill development in clinical research operations.