Clarivate Hiring Associate STEM Content Analyst |Hyderabad/Chennai
- Associate STEM Content Analyst – Clarivate (Hybrid)
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Work Mode
- Why Join Clarivate?
- Application Process
- FAQs
Associate STEM Content Analyst – Clarivate (Hybrid)
Apply for Associate STEM Content Analyst at Clarivate (Hybrid). Openings for BPharm, MPharm, MSc in Life Sciences with 2+ years experience.
Join Clarivate, a global leader in data-driven insights for the life sciences industry, as an Associate STEM Content Analyst. This is a fantastic opportunity for pharma and life sciences professionals looking to advance their career in clinical research analytics, data intelligence, and pharmaceutical R&D. The role is hybrid, offering flexibility, growth, and exposure to global healthcare data systems.
Company Overview
Clarivate is a trusted name in innovation and research intelligence, empowering pharmaceutical and healthcare organizations worldwide. The company provides advanced analytics and insights across drug development, clinical trials, and regulatory landscapes. Its products, including Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence, are used globally to enhance clinical decision-making and improve patient outcomes.
By joining Clarivate, you become part of a collaborative global team dedicated to transforming scientific information into actionable insights that shape the future of medicine.
Job Role & Responsibilities
As an Associate STEM Content Analyst, you will play a crucial role in analyzing, curating, and maintaining accurate data related to clinical trials, pharmaceutical pipelines, and drug development. Your work directly contributes to the quality and credibility of Clarivate’s global data products.
Key Responsibilities:
- Research, analyze, and update clinical trial data from multiple sources including clinical registries, pharma company websites, press releases, and scientific conferences.
- Cross-verify and ensure the accuracy of trial information, drug phase details, and company-level data.
- Track clinical trial performance metrics and maintain records in line with data quality standards.
- Stay updated on emerging trends in drug development and regulatory changes.
- Collaborate with senior analysts and cross-functional teams to meet project deadlines and KPIs.
- Maintain adherence to high-quality standards while managing large datasets.
- Identify training needs and proactively enhance your domain knowledge in life sciences and clinical research.
Eligibility / Qualifications
Required Education:
- B.Pharm, M.Pharm, or MSc in Biotechnology, Microbiology, Life Sciences, or related fields.
Required Experience:
- Minimum 2 years of experience in analyzing and updating clinical reports or trial data.
Key Skills:
- Deep understanding of clinical trial phases, pharmaceutical pipelines, and drug discovery processes.
- Strong research and analytical mindset.
- Excellent written and verbal communication skills in English.
- Ability to handle large volumes of data with precision.
Preferred Skills:
- Experience in secondary research related to clinical and pharmaceutical domains.
- Familiarity with data visualization and medical content management tools.
Location & Work Mode
- Location: Hybrid (Work from Office + Remote flexibility)
- Work Schedule: Monday to Friday (8 hours/day)
- Employment Type: Full-time, Permanent
Why Join Clarivate?
- Be part of a world-leading life sciences data intelligence organization.
- Exposure to global clinical data and healthcare analytics systems.
- Competitive compensation and structured growth path.
- Supportive team culture with opportunities for professional development.
- Contribute to data that drives global medical and pharmaceutical innovation.
Application Process
Interested and qualified candidates can apply directly through the official Clarivate career portal:
👉 Apply Here
Apply as soon as possible to secure your application
FAQs
1. What qualifications are required for this role?
Candidates must hold a BPharm, MPharm, or MSc in Biotechnology, Microbiology, or Life Sciences with at least 2 years of relevant experience.
2. Is this a remote position?
This is a hybrid role offering a mix of remote flexibility and on-site work.
3. What kind of work will I be doing?
You will be involved in analyzing clinical trial data, maintaining data quality, and supporting Clarivate’s intelligence platforms used by global pharma leaders.
4. What is the team structure?
The team includes 20 members comprising Content Specialists, Senior Analysts, and Associate Analysts.
5. How do I apply?
Submit your application through the official Clarivate Careers portal using the link provided above.
| Company | Clarivate |
|---|---|
| Vacancies | Multiple openings |
| Required Education | BPharm, MPharm, MSc (Biotechnology, Microbiology, Life Sciences) |
| Experience | Minimum 2 years in clinical research data analysis |
| Work Type | Full-time, Hybrid |
| Application Link | Apply Here |
To apply for this job please visit careers.clarivate.com.
