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Clinical Research Associate

Lambda Therapeutic Research
Lambda Therapeutic Research
5+ years
500000 - 1000000
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: Clinical Research Associate (CRA)
Req ID: 1491
Date: January 6, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 500,000 – 1,000,000


About Lambda Therapeutic Research Ltd.

Lambda Therapeutic Research Ltd. is a full-service global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategically located facilities in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK), we provide end-to-end clinical research solutions to innovators, biotech firms, and pharmaceutical companies worldwide.

Our mission is to uphold the highest standards of clinical trial management, regulatory compliance, and scientific excellence across diverse therapeutic areas.


Role Overview

We are seeking a Clinical Research Associate (CRA) to oversee site management, patient recruitment, and protocol compliance for ongoing clinical trials. The ideal candidate will have hands-on experience in clinical trial operations, strong communication skills, and the ability to ensure timely and accurate trial execution in collaboration with study sites and internal teams.


Key Responsibilities

  • Provide training to site staff on study protocols, study-related documents, and trial procedures.

  • Conduct site visits, including Site Initiation Visits (SIV), Site Selection Visits (SSV), Monitoring Visits (SMV), and Close-Out Visits (SCOV), as per project scope.

  • Maintain close communication with study sites regarding patient screening, recruitment, follow-up, and other trial-related activities.

  • Ensure compliance with all study requirements and proper documentation at study sites.

  • Monitor timely availability of study materials and Investigational Medicinal Products (IMPs) at the sites.

  • Act as a liaison between Lambda Therapeutic Research teams and clinical sites.

  • Review source data and maintain updated Site Master Files (SMFs).

  • Support internal and external audits by ensuring documentation and trial conduct meet regulatory and organizational standards.


Experience Required

  • Minimum 5 years of experience in the pharmaceutical industry, including at least 1 year as a CRA in clinical trials.

  • Proven knowledge of clinical trial processes, monitoring, and regulatory compliance.


Educational Qualifications

  • MSc, M. Pharm, B. Pharm, BAMS, BHMS, BDS, or equivalent degree in medical or life sciences.


Competencies and Skills

  • Accountability and ownership of responsibilities

  • Strong communication and presentation skills

  • Professional work ethic and integrity

  • Initiative and problem-solving skills

  • Technical knowledge of clinical trial processes

  • Motivation, interpersonal, and leadership skills

  • Planning, organizing, and flexibility in dynamic trial environments

  • Ability to align with organizational culture and team collaboration


Why Join Lambda Therapeutic Research?

  • Opportunity to work in a global CRO with exposure to international clinical trials and regulatory standards.

  • Hands-on experience in site management, monitoring, and patient recruitment across therapeutic areas.

  • Career growth through mentorship, cross-functional training, and exposure to global clinical operations.