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Research Associate

Lambda Therapeutic Research
Lambda Therapeutic Research
2-3 years
INR 4,00,000 – 5,00,000
10 Oct. 7, 2025
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

Req ID: 1213
Date Posted: September 29, 2025
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 4,00,000 – 5,00,000


Organizational Overview

Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with facilities in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK).

Key Highlights:

  • Provides end-to-end clinical research services for innovator, biotech, and generic pharmaceutical industries


Department: Bioanalytical Operations

Designation: Research Associate
Education Required: M.Pharm / B.Pharm / M.Sc.
Experience Required: 2 – 3 years


Job Overview

The Research Associate will work in bioanalytical operations, focusing on method development, sample analysis, and instrument handling in compliance with regulatory standards and GLP principles.


Key Responsibilities

  • Develop and validate bioanalytical methods

  • Process and analyze samples for assigned projects

  • Operate, calibrate, and troubleshoot LC-MS/MS instruments and other analytical instruments

  • Prepare draft SOPs and methods; work in compliance with system/method-specific SOPs and study protocols

  • Ensure proper training on SOPs/documents prior to performing related activities

  • Ensure effective implementation of GLP and 21 CFR Part 11:

    • Check instrument labels

    • Maintain logbooks for equipment and instruments

    • Ensure instruments are calibrated before due date

  • Follow OECD GLP principles in all activities


Required Competencies

  • Accountability

  • Communication

  • Work Ethic

  • Presentation / Communication Skills

  • Organizational Culture Fit