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Research Associate

Lambda Research Accelerated
Lambda Research accelerated
2-3 years
4,00,000 – 5,00,000
10 Jan. 2, 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

Research Associate – Bioanalytical Operations

Location: Ahmedabad, Gujarat, India
Employment Type: Full-Time
Experience Required: 2–3 years
CTC Range: INR 4,00,000 – 5,00,000 per annum
Job ID: 1213


Company Overview

Lambda Therapeutic Research Ltd. is a globally established, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operational centers across India, the United States, Canada, Poland, and the United Kingdom, Lambda delivers comprehensive clinical, bioanalytical, and regulatory research services to innovator, biotech, and generic pharmaceutical companies worldwide.

Driven by scientific rigor, regulatory compliance, and quality excellence, Lambda supports end-to-end drug development programs across multiple therapeutic areas.


Role Overview

Lambda Therapeutic Research is seeking a motivated Research Associate – Bioanalytical Operations to join its Bioanalytical team in Ahmedabad. This role is ideal for professionals with hands-on experience in bioanalytical method development and validation who are looking to advance their careers within a GLP-compliant, global research environment.


Key Responsibilities

  • Develop and validate bioanalytical methods in accordance with regulatory and study requirements.

  • Perform sample processing and analysis for assigned bioanalytical studies.

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

  • Prepare and review draft analytical methods and method-specific SOPs.

  • Ensure strict adherence to system-, method-, and study-specific SOPs, protocols, and plans.

  • Maintain compliance with GLP, OECD GLP principles, and 21 CFR Part 11 requirements.

  • Verify instrument labeling, calibration status, and completeness of equipment logbooks.

  • Ensure completion of required SOP and compliance training prior to initiating laboratory activities.


Experience & Skills

  • 2–3 years of relevant experience in bioanalytical method development, validation, and sample analysis.

  • Practical expertise in LC–MS/MS instrumentation and regulated laboratory operations.

  • Working knowledge of GLP, OECD GLP, and 21 CFR Part 11 compliance requirements.

  • Strong attention to detail, documentation accuracy, and data integrity.

  • Effective written and verbal communication skills.


Educational Qualifications

  • M.Pharm, B.Pharm, or M.Sc. in Pharmaceutical Sciences, Analytical Chemistry, or a related discipline.


Core Competencies

  • Accountability and ownership of assigned responsibilities

  • Strong communication and presentation skills

  • High work ethic with a quality-focused mindset

  • Effective time management and organizational skills

  • Alignment with organizational values and collaborative culture


Why Join Lambda Therapeutic Research?

  • Opportunity to work within a globally recognized CRO environment

  • Exposure to international regulatory standards and advanced bioanalytical platforms

  • Competitive compensation aligned with experience and expertise

  • Professional growth within a structured, compliance-driven research setting


Apply Today
Advance your bioanalytical research career with Lambda Therapeutic Research Ltd. and contribute to high-impact global clinical development programs.