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Stem Content Analyst

2+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Pharm./M.Pharm/MSc 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

STEM Content Analyst - JREQ131835
Location: Tamil Nadu, India (Hybrid)
Department: Life Sciences & Healthcare
Job Type: Permanent contract


About the Role

We are looking for a STEM Content Analyst to join our team at Clarivate. In this role, you will focus on analyzing and updating clinical trial data and content related to pharmaceutical pipelines, drug development, and clinical phases. You will work on secondary research to curate accurate clinical trial records and contribute to the development of insights that will support drug safety and discovery intelligence.


Responsibilities

  • Analyze and update clinical trial information from various sources, including company websites, presentations, conferences, press releases, and clinical trial repositories.

  • Record and track performance against targets, ensuring the accuracy and timeliness of the updates.

  • Contribute to team collaboration to meet content-related goals and ensure the quality of deliverables.

  • Maintain awareness of developments in clinical trial technology and pharmaceutical research.

  • Take responsibility for identifying personal training and developmental needs on an ongoing basis.

  • Adapt to process changes and contribute to process improvement within the team.


Qualifications & Experience

Required:

  • Education: BPharm, MPharm, MSc in Biotechnology, Microbiology, Life Sciences, or related fields.

  • Experience: At least 2 years of experience in analyzing and updating clinical reports.

  • Skills:

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

    • Excellent communication skills (written and verbal) in English.

    • Strong ability to conduct secondary research related to clinical information.

Preferred:

  • Ability to work independently and in collaboration with peers across different teams.

  • Attention to detail and the ability to handle complex datasets.


About the Team

You will join the team working on the Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence products. The team consists of 20 content specialists, senior content analysts, content analysts, and associate content analysts.


Work Hours

  • Hybrid work mode: Monday to Friday

  • Working Hours: 8 hours per day (Full-Time, Permanent)


Equal Employment Opportunity

Clarivate is committed to providing equal employment opportunities for all qualified individuals and ensuring a non-discriminatory and inclusive work environment.