STEM Content Analyst – Drug Development Research
Location: Hyderabad, Telangana, India
Work Mode: Hybrid
Department: Life Sciences & Healthcare
Job ID: JREQ134431
Employment Type: Full-Time
Working Hours: 9:00 AM – 6:00 PM IST (40 hours per week)
About the Role
A leading global life sciences information organization is seeking a STEM Content Analyst to join its CDDI Drugs Team in Hyderabad, India. This role offers a strong opportunity for professionals interested in drug development research, pharmaceutical competitive intelligence, clinical trial analysis, and structured drug data management.
The selected candidate will work within a collaborative international team spanning India and Spain, contributing to high-quality drug development insights used by researchers, scientists, and healthcare stakeholders worldwide.
This position is ideal for professionals with a background in pharmacy and experience in secondary research, competitive intelligence, and pharmaceutical content analysis.
Experience Required
Minimum 2 years of relevant experience in:
Secondary market research
Pharmaceutical competitive analysis
Drug development intelligence
Healthcare content analysis
Educational Qualification (Mandatory)
M.Pharm, B.Pharm, or D.Pharm degree
Key Responsibilities
As a STEM Content Analyst, you will:
Analyze drug-related references including:
Clinical trial data
Company and research institution press releases
Regulatory documentation (FDA, EMA, and other global agencies)
Company pipelines and public disclosures
Identify and track:
New drug entries
Drug development updates
Clinical phase transitions
Target indications and formulations
Organizations involved in development
Produce structured and high-quality drug summaries covering:
Mechanism of Action (MoA)
Product classification
Development status
Regulatory milestones
Target diseases
Drug activity insights
Conduct comprehensive online research to identify reliable pharmaceutical sources
Summarize and edit complex scientific information with accuracy and clarity
Meet defined weekly production and quality KPIs
Contribute to continuous process improvements
Collaborate with cross-functional and international teams
Adapt to workflow and process updates
Execute additional assignments as directed by the reporting manager
Required Skills & Competencies
Strong knowledge of pharmaceutical content analysis and editing
Understanding of drug development lifecycle from patent to market access
Excellent written and verbal communication skills
Strong analytical and critical thinking abilities
Ability to work independently and within a team environment
Adherence to SOPs and compliance policies
Capability to manage deadlines in fast-paced environments
Proficiency in Microsoft Office (Word, Excel, PowerPoint)
Preferred Skills (Good to Have)
Practical use of AI tools for research and content enhancement
Basic knowledge of SQL and/or Python for data analysis
Familiarity with global regulatory databases and pharmaceutical intelligence platforms
About the Drug Development Team
The Drug Development Team specializes in analyzing:
Global clinical trials
Pharmaceutical company pipelines
Regulatory agency disclosures
Institutional research updates
The team delivers structured, validated drug intelligence content used by scientists and healthcare professionals researching therapeutic advancements.
Team Locations:
India: Bengaluru, Hyderabad, Chennai
Spain: Barcelona
Why Apply?
Work on global pharmaceutical intelligence projects
Gain exposure to international drug development data
Collaborate with cross-border experts in life sciences
Build expertise in clinical research analytics and competitive intelligence
Equal Opportunity Statement
The organization is committed to providing equal employment opportunities in hiring, promotion, compensation, and professional development. All qualified candidates will receive consideration in accordance with applicable employment laws and regulations.
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