Clarivate is hiring Associate STEM Content Analyst (Associate Content Editor – Clinical Studies) for its Hyderabad office. This opportunity is ideal for B.Pharm, M.Pharm, and M.Sc (Biotechnology/Microbiology) graduates looking to build a career in clinical trials intelligence, drug development research, and pharmaceutical data analysis.
The selected candidates will work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence, two globally recognized platforms supporting pharmaceutical R&D, clinical research, and regulatory strategy.
If you are searching for clinical research jobs in Hyderabad for freshers, BPharma jobs in IT companies, or clinical data analysis roles in pharma, this hybrid opportunity at Clarivate is highly relevant.
Job Overview
- Job Title: Associate STEM Content Analyst (Clinical Studies)
- Company: Clarivate
- Location: Hyderabad (Hybrid – Mon–Fri)
- Experience: Freshers or 0–6 months
- Qualification: B.Pharm / M.Pharm / M.Sc (Biotechnology, Microbiology, Chemistry)
- Work Hours: 9:00 AM – 6:00 PM
- Employment Type: Full-Time, Permanent
Key Responsibilities
As an Associate STEM Content Analyst in the Clinical team, you will:
- Maintain and update Clarivate’s database with accurate clinical trials information
- Analyze and cross-reference data from:
- Clinical trial registries
- Scientific meetings & conferences
- Press releases
- Public pharmaceutical pipeline sources
- Interpret complex data related to:
- Drug development stages
- Clinical trial phases (Phase I–IV)
- Investigational products and marketed drugs
- Deliver weekly productivity targets
- Ensure strict quality control standards
- Perform secondary research related to clinical studies and drug pipelines
This role strengthens your foundation in clinical intelligence, pharmaceutical drug pipelines, and global trial data tracking.
Required Qualifications
Educational Qualification
- B.Pharm (Pharmaceutical Analysis & QA preferred)
- M.Pharm
- M.Sc (Biotechnology, Microbiology, Chemistry)
Experience
- Freshers welcome
- OR up to 6 months experience in clinical report analysis or updating clinical records
Required Skills
- Strong knowledge of:
- Clinical trials processes
- Drug development lifecycle
- Pharmaceutical pipelines
- Clinical phases (Phase I–IV)
- Excellent English written & verbal communication
- Analytical mindset and problem-solving ability
- Ability to interpret complex clinical study data
Preferred Skills
- Experience in secondary research on clinical data
- Familiarity with pharmaceutical databases
- Basic understanding of global regulatory frameworks
Why Join Clarivate?
Working at Clarivate offers:
- Exposure to global pharmaceutical R&D data
- Hands-on experience in Cortellis platforms
- Hybrid work model (work-life balance)
- Stable IT services & consulting environment
- Career pathway into:
- Clinical Research
- Regulatory Intelligence
- Drug Development Analytics
- Medical Writing
- Pharma Data Science
This position is particularly valuable for candidates targeting long-term careers in clinical intelligence, drug discovery analytics, and regulatory research.
Salary (Estimated)
Based on market standards for Hyderabad IT-pharma hybrid roles:
₹3,00,000 – ₹4,50,000 per annum (CTC)
(Final offer may vary based on qualification and internal policy)
How to Apply
