STEM Content Analyst – Drug Development Research
Location: Hyderabad, Telangana, India
Work Mode: Hybrid
Employment Type: Full-Time
Industry: Life Sciences & Healthcare
Experience Required: Minimum 2+ Years (Secondary Research / Pharmaceutical Analysis)
Job Overview
A leading global life sciences information organization is hiring a STEM Content Analyst to join its Drug Development Intelligence team in Hyderabad. This role focuses on pharmaceutical research, clinical trial analysis, competitive intelligence, regulatory tracking, and structured drug data curation.
The selected candidate will contribute to drug pipeline monitoring, clinical research analysis, regulatory intelligence, and scientific content development supporting global healthcare and pharmaceutical stakeholders. This position is ideal for pharmacy graduates with experience in secondary market research, drug analysis, and pharmaceutical content management.
Key Responsibilities
Analyze drug-related references including clinical trials, regulatory approvals, company press releases, and research publications
Monitor regulatory updates from agencies such as FDA and EMA
Identify new drugs and track updates including development phase, mechanism of action, target indication, formulation, and sponsoring organizations
Conduct comprehensive online research to gather drug development intelligence
Summarize, edit, and structure pharmaceutical content accurately and clearly
Maintain weekly production and quality KPIs
Collaborate with cross-functional and global teams on research deliverables
Contribute to continuous process improvement initiatives
Ensure adherence to SOPs, editorial standards, and internal quality policies
Required Qualifications
Education:
M.Pharm, B.Pharm, or D.Pharm is mandatory.
Experience:
Minimum 2 years of relevant experience in secondary market research, pharmaceutical competitive intelligence, drug pipeline analysis, or healthcare research.
Technical Skills:
Strong understanding of drug development lifecycle
Knowledge of clinical trials and regulatory processes
Experience in content analysis and editing
Proficiency in Microsoft Office (Word, Excel, PowerPoint)
Ability to meet strict deadlines and production targets
Preferred Skills:
Proficiency in AI tools for research and productivity enhancement
Basic knowledge of SQL or Python
Exposure to pharmaceutical databases
Core Competencies:
Strong analytical and research skills
Excellent written and verbal communication
High attention to detail and accuracy
Ability to work independently and in team-based environments
Adaptability to process changes
About the Team
The Drug Development Intelligence team specializes in analyzing clinical trials, regulatory filings, company announcements, research publications, and pharmaceutical pipelines. The team produces structured drug intelligence content including:
Mechanism of Action (MoA)
Product categories
Development status
Target diseases
Regulatory milestones
Comprehensive drug summaries
The team operates across multiple global locations including Hyderabad, Bengaluru, Chennai, and Barcelona, supporting international pharmaceutical and life sciences clients.
Work Schedule
Full-Time Position
40 hours per week
9:00 AM to 6:00 PM IST
Hybrid work model
Equal Opportunity Statement
The organization is committed to providing equal employment opportunities to all qualified candidates and adheres to applicable employment and non-discrimination laws
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