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Associate Stem Content Analyst

2+ years
Not Disclosed
10 Oct. 13, 2025
Job Description
Job Type: Full Time Hybrid 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

Associate STEM Content Analyst

Job ID: JREQ133450
Posted Date: August 20, 2025
Location: Two locations (Not specified)
Division: Life Sciences & Healthcare
Work Mode: Hybrid
Work Hours: 8 hours/day, Monday to Friday
Employment Type: Full-Time, Permanent


Summary

The Associate STEM Content Analyst will join Clarivate’s Clinical Trial Intelligence and Drug Discovery Intelligence team. The role involves analyzing, updating, and cross-referencing clinical trial information from multiple sources to ensure high-quality, up-to-date content.


Key Responsibilities

  • Actively seek out and collect information on clinical trials from company websites, presentations, conferences, press releases, clinical trial repositories, and other sources

  • Analyze and cross-reference data to update clinical trial records

  • Maintain awareness of current developments in relevant technology and therapeutic areas

  • Ensure targets and quality standards are consistently met

  • Take responsibility for personal planning, time management, and ongoing professional development

  • Adapt flexibly to process changes and new technologies

  • Undertake additional reasonable duties as requested by the line manager or director


Qualifications & Experience

Required

  • Bachelor’s or Master’s degree in Pharmacy (BPharm/MPharm), Biotechnology, Microbiology, or Life Sciences

  • Minimum 2 years of experience in analyzing and updating clinical reports

  • In-depth knowledge of clinical trials, drug pipelines, drug development, and clinical trial phases

  • Excellent written and verbal English communication skills

Preferred / Desirable

  • Experience in secondary research related to clinical information

  • Strong analytical skills with attention to detail and the ability to delve deeply into content and results


About the Team

  • Works on Clarivate’s Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence products

  • Team size: ~20 members, including Content Specialists, Senior Content Analysts, Content Analysts, and Associate Content Analysts


Work Environment & Culture

  • Monday to Friday, full-time

  • Hybrid work mode

  • Equal employment opportunity employer, committed to diversity and inclusion

  • Compliance with all applicable non-discrimination laws and regulations