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Associate Stem Content Analyst

0-1 years
Not Disclosed
10 Oct. 6, 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

Job Title: Associate STEM Content Analyst

📍 Location: Hyderabad, Telangana, India
🏢 Department: Life Sciences & Healthcare
🖥️ Work Mode: Hybrid
🆔 Job ID: JREQ133654
📅 Posted Date: September 11th, 2025


About the Role

We are seeking an Associate Content Editor to join our Clinical Studies team in Hyderabad. This is an excellent opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence platforms.

As an Associate Content Editor, you will be responsible for collecting, analyzing, cross-referencing, and updating clinical study information from diverse sources, including:

  • Scientific meetings and conferences

  • Trial registries

  • Press releases

  • Other credible internet sources

You will ensure that Clarivate’s clinical records remain accurate, up-to-date, and comprehensive.


Key Responsibilities

  • Maintain Clarivate’s database with current and accurate clinical trial information.

  • Collect and interpret data from multiple sources.

  • Analyze and update information related to clinical trials, drugs, and therapeutic areas.

  • Meet weekly delivery targets and ensure high-quality data standards.

  • Understand and interpret complex trial and drug-related content.

  • Demonstrate strong analytical and problem-solving skills.


About You

🎓 Education:

  • B.Pharm / M.Pharm / M.Sc in Biotechnology, Microbiology, or related life science fields

💼 Experience:

  • 0–1 year of experience in analyzing and updating clinical reports

🧠 Knowledge & Skills:

  • In-depth understanding of:

    • Clinical trials and phases

    • Pharmaceutical drug pipelines

    • Drug development process

  • Excellent English communication skills (written & verbal)

  • Strong attention to detail and accuracy


Preferred Qualifications

  • Experience in secondary research related to clinical information


Work Schedule

🗓️ Days: Monday to Friday
Hours: 9:00 AM – 6:00 PM IST
🏠 Mode: Hybrid


Equal Opportunity Statement

At Clarivate, we are committed to providing equal employment opportunities for all qualified individuals regarding hiring, compensation, promotion, training, and other employment conditions. We fully comply with applicable non-discrimination laws and regulations across all locations.