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Associate Stem Content Analyst

2+ years
Not Disclosed
10 Sept. 18, 2025
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: Associate STEM Content Analyst

📍 Locations: 2 (Hybrid – Remote)
🆔 Job ID: JREQ133450
📅 Posted Date: August 20, 2025
🏢 Business Unit: Life Sciences & Healthcare


Role Overview

The Associate STEM Content Analyst will be responsible for analyzing and updating clinical trial records by gathering and verifying information from diverse sources. The role requires strong knowledge of clinical trials, drug pipelines, and pharmaceutical development processes, along with excellent communication and research skills.


Education & Qualifications

  • B.Pharm / M.Pharm / M.Sc. in Biotechnology, Microbiology, or Life Sciences


Experience

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

  • Knowledge of clinical trials, drug pipelines, drug development, and clinical phases


Key Skills

  • Strong English written and verbal communication

  • Analytical skills with attention to detail

  • Effective personal planning and time management

  • Flexibility and adaptability to process changes


Preferred Skills (Good to Have)

  • Experience in secondary research related to clinical information

  • Ability to delve deep into scientific content and interpret results


Responsibilities

  • Seek, analyze, cross-reference, and update clinical trial information from multiple sources including company websites, presentations, conferences, press releases, clinical trial repositories, and other internet sources

  • Maintain and update accurate clinical trial records

  • Record performance against targets and actively contribute to achieving team goals

  • Stay updated on current developments in assigned therapeutic or technology areas

  • Ensure consistent quality standards in all deliverables

  • Take responsibility for identifying personal training and development needs

  • Support process improvements with a flexible and adaptable approach

  • Undertake any other duties assigned by the Line Manager/Director on a permanent or temporary basis


About the Team

The role is part of the Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence product team. The team consists of ~20 members, including Content Specialists, Senior Content Analysts, Content Analysts, and Associate Content Analysts.


Work Hours

  • Full-Time, Permanent

  • 8 hours per day, Monday to Friday


Equal Opportunity

Clarivate is committed to providing equal employment opportunities to all qualified persons regardless of race, religion, sex, color, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions are based on business needs, merit, and qualifications, in compliance with applicable laws and regulations.


Impact: Your work will directly support accurate, high-quality clinical intelligence for pharmaceutical and healthcare research, enabling better decision-making in drug development.