Associate STEM Content Analyst – Clinical Trials & Drug Intelligence
Location: Hyderabad, Telangana, India
Work Model: Hybrid (Monday–Friday)
Working Hours: 9:00 AM – 6:00 PM IST
Employment Type: Full-Time
Industry: Life Sciences & Healthcare – Clinical Research & Drug Development
Job ID: JREQ134953
Posted Date: February 16, 2026
The Pharma Daily is inviting applications for the position of Associate STEM Content Analyst to join a Clinical Studies team in Hyderabad. This opportunity is ideal for life sciences graduates who are interested in clinical trials intelligence, drug development research, and pharmaceutical pipeline analysis.
The selected candidate will contribute to globally recognized clinical and drug intelligence databases by monitoring, analyzing, and updating structured clinical trial information. This role is suited for candidates who have strong knowledge of clinical research processes and pharmaceutical development stages.
Experience Required
Freshers or candidates with up to 6 months of relevant experience in clinical research, clinical data analysis, or healthcare content analysis.
Exposure to analyzing and updating clinical reports or drug pipeline information is an advantage.
Basic understanding of secondary research related to clinical and pharmaceutical information is preferred.
Educational Qualifications
B.Pharm, M.Pharm, or M.Sc. in Biotechnology, Microbiology, or related Life Sciences disciplines.
Core Skills and Competencies
Strong knowledge of clinical trials, drug development lifecycle, and clinical phases (Phase I–IV).
Understanding of pharmaceutical drug pipelines and regulatory development processes.
Ability to interpret complex clinical study data from multiple sources.
Excellent written and verbal communication skills in English.
Strong analytical and problem-solving mindset.
Attention to detail with a focus on data accuracy and quality compliance.
Ability to meet weekly production targets in a structured content environment.
Key Responsibilities
Monitor and collect clinical trial and drug-related information from scientific meetings, conferences, trial registries, press releases, and credible online sources.
Analyze, cross-reference, and update clinical study records in internal databases.
Maintain high standards of accuracy and ensure clinical intelligence content is current and reliable.
Interpret complex trial designs, endpoints, and drug development data.
Meet defined productivity and quality benchmarks on a weekly basis.
Ensure compliance with editorial and database management standards.
About the Team
The Clinical Studies team consists of approximately 20 professionals specializing in clinical trial intelligence and drug discovery data analysis. The team supports global pharmaceutical and biotechnology organizations by delivering structured, high-quality clinical insights to enable informed strategic decision-making.
Equal Employment Opportunity
The employer is committed to providing equal employment opportunities to all qualified individuals in hiring, compensation, promotion, training, and all other employment-related practices in accordance with applicable laws and regulations.
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