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Associate Stem Content Analyst

0-1 years
Not Disclosed
10 Oct. 31, 2025
Job Description
Job Type: 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 On: September 11th, 2025


About the Role

Clarivate is seeking an Associate Content Editor to join the Clinical Studies team in Hyderabad. This is an exciting opportunity to contribute to Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence platforms.
You will be responsible for collecting, analyzing, and updating clinical study data from diverse and credible sources such as scientific conferences, trial registries, press releases, and online databases.


Key Responsibilities

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

  • Collect, analyze, and cross-reference data from multiple sources (e.g., scientific meetings, registries, press releases).

  • Ensure timely completion of weekly data targets.

  • Maintain high-quality standards for accuracy and completeness.

  • Interpret and summarize complex clinical and drug development information.

  • Demonstrate analytical and problem-solving abilities to identify data inconsistencies.


Qualifications & Requirements

Education

  • B.Pharm / M.Pharm / M.Sc. (Biotechnology, Microbiology, or related Life Science disciplines)

Experience

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

Knowledge & Skills

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

  • Strong written and verbal communication skills in English.

  • Good analytical reasoning and data interpretation abilities.


Preferred Skills

  • Experience in secondary research related to clinical or pharmaceutical information.


Work Schedule

  • Days: Monday to Friday

  • Hours: 9:00 AM – 6:00 PM IST

  • Mode: Hybrid (Work from Office + Remote flexibility)


About Clarivate

Clarivate is committed to providing equal employment opportunities to all qualified individuals. We comply with applicable laws on non-discrimination and ensure fair practices in all employment processes, including hiring, promotion, and compensation.