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Research Associate

Lambda Research Accelerated
Lambda Research accelerated
4-5 years
3,50,000 – 5,50,000
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

Job Title: Research Associate – Clinical Laboratory
Location: Ahmedabad, Gujarat, India
Employment Type: Full-Time
CTC Range: INR 3,50,000 – 5,50,000 per annum
Experience Required: 4–5 years


Company Overview

Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with strategic operations in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland). Lambda provides comprehensive end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide, delivering high-quality clinical laboratory testing, regulatory compliance, and operational excellence.


Role Overview

Lambda Therapeutic Research is seeking a skilled Research Associate for its Clinical Laboratory in Ahmedabad. This role involves managing laboratory instruments, conducting clinical sample testing, analyzing quality control results, and ensuring compliance with standard operating procedures (SOPs) and quality standards. The ideal candidate will have 4–5 years of hands-on experience in clinical laboratory operations and strong expertise in hematology, biochemistry, coagulation, and urine analysis.


Key Responsibilities

  • Operate and maintain hematology, biochemistry, coagulation, and urine analyzers.

  • Conduct testing of QC, patient, subject, and EQAS samples according to defined SOPs.

  • Analyze and evaluate EQAS sample results, ensuring timely reporting.

  • Update section in-charge regarding stock, inventory, and consumable requirements on a monthly or as-needed basis.

  • Perform routine instrument maintenance and troubleshoot operational issues as required.

  • Execute sample accession activities, including temperature monitoring and instrument data backup.

  • Maintain laboratory documentation, records, and logs accurately in compliance with regulatory standards.

  • Assist in implementing quality improvement initiatives in the clinical laboratory.

  • Undertake any additional responsibilities assigned by management or Head of Department (HOD).


Experience & Qualifications

  • Experience: Minimum 4–5 years in clinical laboratory operations, preferably in a CRO or hospital laboratory environment.

  • Education: B.Sc., M.Sc., or Medical Laboratory Technology (MLT) qualification.

  • Proficiency in hematology, biochemistry, coagulation, and urine analysis procedures.

  • Knowledge of quality control practices, EQAS sample handling, and SOP compliance.

  • Strong analytical and problem-solving skills with high attention to detail.

  • Excellent organizational and time management skills.

  • Effective communication and teamwork skills in a multidisciplinary environment.


Why Join Lambda Therapeutic Research?

  • Work with a global CRO providing clinical research services across multiple countries.

  • Gain exposure to international laboratory standards, regulatory compliance, and clinical research best practices.

  • Opportunity for professional growth and skill development in clinical laboratory operations.

  • Collaborate with a highly skilled team of scientists and clinical research experts.

  • Competitive compensation and a supportive, performance-driven work environment.


Apply Today: Advance your career in clinical research with Lambda Therapeutic Research, contributing to high-quality laboratory testing and global clinical trial success.