Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Technical Officer - Clinical Data Coordinator

Lambda Research Accelerated
Lambda Research accelerated
1-3 years
INR 3,00,000 – 6,00,000 per annum
Ahmedabad, India
10 March 6, 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

Technical Officer – Clinical Data Coordinator

Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
Salary Range: INR 3,00,000 – 6,00,000 per annum
Experience Required: 1–3 years
Employment Type: Full-Time

About Lambda Therapeutic Research Ltd.
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The company provides comprehensive end-to-end clinical research services to pharmaceutical, biotechnology, and generic drug companies worldwide. Lambda operates advanced clinical research facilities across multiple locations including Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), supporting global drug development programs and regulatory submissions.

Key Responsibilities

  • Develop and test electronic Case Report Forms (eCRFs) to ensure accurate clinical data capture and compliance with study protocols.

  • Perform clinical data validation and manage data queries to maintain high-quality and consistent clinical trial datasets.

  • Prepare and maintain Clinical Data Management documentation including Data Management Plan (DMP), Data Validation Plan (DVP), and electronic Case Completion Guidelines (eCCG).

  • Conduct data reconciliation activities and support training related to data management processes and systems.

  • Perform medical coding activities using standard coding dictionaries and tools.

  • Collaborate with clinical research teams to ensure timely data review, issue resolution, and database integrity during clinical trials.

Experience Required

  • 1–3 years of relevant experience in clinical data management or clinical research coordination.

  • Prior site-level experience as a Clinical Research Coordinator for late-phase clinical trials is preferred.

  • Hands-on experience with Electronic Data Capture (EDC) systems and related tools such as IWRS and ePRO.

  • Familiarity with clinical data management workflows including data cleaning, reconciliation, and query handling.

Educational Qualification

  • M.Pharm (Pharmacology / Quality Assurance)

  • BDS / BAMS / BHMS

  • M.Sc. in Life Sciences

Why Join Lambda Therapeutic Research

  • Opportunity to work with a globally recognized CRO supporting international clinical research programs.

  • Exposure to advanced clinical data management systems and global regulatory environments.

  • Collaborative work environment focused on scientific innovation and professional growth.