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Clarivate, a global leader in life sciences and healthcare research intelligence, is hiring an Associate STEM Content Analyst. This is a fantastic opportunity for professionals with a background in pharma, biotechnology, or life sciences to contribute to global clinical trial intelligence.
This role offers a hybrid work model, competitive compensation, and the chance to be part of a team powering Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence.
🔹 Job Responsibilities
As an Associate STEM Content Analyst, you will:
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- Research, analyze, and update clinical trial records from reliable sources such as company websites, press releases, conferences, and repositories.
- Cross-reference trial data to ensure accuracy and consistency.
- Record and track performance against targets.
- Maintain awareness of the latest developments in drug pipelines and clinical trial phases.
- Collaborate with team members to meet deadlines and quality standards.
- Adapt to evolving processes while ensuring consistent reporting accuracy.
- Take ownership of personal skill development and training needs.
🔹 Qualifications & Skills
- Education: B.Pharm, M.Pharm, or MSc (Biotechnology, Microbiology, Lifesciences).
- Experience: Minimum 2 years in analyzing or updating clinical reports.
- Strong understanding of clinical trials, drug development, and pharmaceutical pipelines.
- Excellent written and verbal English communication skills.
Preferred:
- Experience in secondary research of clinical trial information.
- Ability to critically analyze trial outcomes and data.
🔹 Benefits of Working at Clarivate
- Competitive salary package (₹5.5 – ₹8 LPA).
- Hybrid working model for flexibility.
- Exposure to global clinical intelligence platforms.
- Learning and growth opportunities in a research-driven environment.
- Inclusive workplace with equal employment opportunities.
🔹 How to Apply
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