Clarivate is hiring an Associate STEM Content Analyst in Hyderabad to join their Clinical Studies team. This is an excellent opportunity for fresh BPharma, MPharma, or MSc graduates to contribute to clinical trials database management and drug discovery intelligence. If you are passionate about clinical research, pharmaceutical drug pipelines, and data analysis, this role is perfect for you.
Responsibilities
As an Associate Content Analyst, you will:
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- Actively gather information about clinical studies from scientific meetings, trial registries, press releases, and other sources.
- Analyze, cross-reference, and update clinical records in the Clarivate database.
- Ensure weekly targets are met with high accuracy and quality standards.
- Interpret complex trial and drug information for database updates.
- Support the team in maintaining up-to-date clinical trials information.
- Apply strong analytical and problem-solving skills to verify and correct clinical data.
Qualifications
Educational Requirements:
- BPharma, MPharma, or MSc in Biotechnology / Microbiology.
Experience:
- 0-1 year of experience in analyzing and updating clinical reports.
Skills & Abilities:
- In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases.
- Excellent written and verbal English communication.
- Strong attention to detail and ability to interpret complex data.
- Experience in secondary research related to clinical information is a plus.
Benefits
- Hybrid working model in Hyderabad.
- Opportunity to work with Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence.
- Skill development in clinical data management and pharma research.
- Collaborative work environment with a team of 20 clinical experts.
How to Apply
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