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Associate Stem Content Analyst

2+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: BPharm/MPharm/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

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


About the Role

We are seeking an Associate STEM Content Analyst to join our Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence team. In this role, you will analyze and update clinical trial reports from various sources, ensuring that the information is accurate and up-to-date. You will also collaborate with the team to meet targets, maintain consistent quality standards, and contribute to the overall success of the team.


Responsibilities

  • Actively seek out information about clinical trials, analyze, cross-reference, and update records with the latest information from sources such as company websites, presentations, conferences, press releases, clinical trial repositories, and other internet sources.

  • Record and track performance against targets to ensure the team achieves its objectives.

  • Take an active role within the team to ensure targets are met consistently.

  • Stay informed of developments in clinical trials and related technology areas.

  • Maintain consistent quality standards while managing your time effectively.

  • Adapt to process changes and maintain a flexible approach.

  • Identify personal technology training and development needs and pursue ongoing growth.

  • Undertake additional duties as requested by your line manager/director, both on a permanent and temporary basis.


Qualifications & Experience

Required:

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

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

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

  • Excellent written and verbal communication skills in English.

Desired:

  • Experience in secondary research related to clinical information.

  • Ability to analyze content in-depth and generate meaningful insights.


About the Team

You will be part of a team working on Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence, with a group size of around 20 members, including Content Specialists, Senior Content Analysts, and Content Analysts. The team culture emphasizes collaboration, accuracy, and continuous improvement.


Work Hours

  • Full-Time: 8 hours per day

  • Hybrid Work: Monday to Friday


Equal Employment Opportunity

Clarivate is committed to providing equal employment opportunities to all individuals, regardless of their background. We adhere to all applicable laws and regulations governing non-discrimination in employment.