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Clinical Data Analyst

2-3 years
Not Disclosed
10 May 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Clinical Data Analyst


Job Summary

We are currently seeking a skilled and detail-oriented Clinical Data Analyst to support clinical trial data analysis and reporting. The successful candidate will create and validate datasets, tables, and figures, lead project efforts, and contribute to the overall data strategy in compliance with clinical and regulatory standards.


Key Responsibilities

  • Create efficacy and safety tables, listings, and figures (TLFs) for clinical trial data

  • Develop derived data specifications and datasets

  • Create and validate SAS macros and utilities to support data analysis

  • Manage multiple clinical projects concurrently and ensure timely delivery of deliverables

  • Lead a team when required and independently execute tasks based on Statistical Analysis Plans (SAP) with minimal biostatistician guidance


Desirable Skills and Experience

  • 2.5–3 years of experience in clinical data analysis

  • Strong understanding of the clinical development process

  • Ability to navigate regulatory environments and ensure data quality under compliance standards

  • SAS programming proficiency; SAS certification is highly desirable

  • Experience managing timelines and project priorities

  • Ability to work independently and as part of a team

  • Solid problem-solving and analytical skills