Associate STEM Content Analyst – Drug Development
Location: Hyderabad, Telangana, India
Work Model: Hybrid (Monday to Friday)
Job ID: JREQ134349
Industry: Life Sciences & Healthcare Analytics
Employment Type: Full-Time
Associate STEM Content Analyst Jobs in Hyderabad – Life Sciences & Drug Development Research
A leading global life sciences information and analytics organization is seeking an Associate STEM Content Analyst to join its Drug Development Intelligence team in Hyderabad, India. This hybrid opportunity is ideal for pharmacy graduates or early-career life sciences professionals interested in clinical trials analysis, drug pipeline tracking, regulatory intelligence, and competitive pharmaceutical research.
This role offers exposure to global drug development data, including clinical trial intelligence, regulatory updates (FDA, EMA), company press releases, and pharmaceutical pipeline analytics.
Role Overview
The Associate STEM Content Analyst will support comprehensive drug development research by analyzing, structuring, and summarizing complex pharmaceutical data. The role involves monitoring clinical trials, identifying drug pipeline updates, and producing structured content related to mechanisms of action, regulatory milestones, target diseases, and development phases.
The position requires analytical thinking, strong content editing capabilities, and the ability to meet production and quality KPIs within a structured research environment.
Key Responsibilities
Drug & Clinical Research Analysis
Analyze drug-related references including:
Clinical trial registries
Regulatory updates from FDA, EMA, and global authorities
Company and research institution press releases
Pharmaceutical pipeline disclosures
Identify new drugs and track updates such as:
Development phase
Target disease
Mechanism of action
Formulation
Sponsoring organizations
Content Structuring & Quality Assurance
Summarize and edit scientific content without grammatical or conceptual errors
Conduct comprehensive online research for drug-related intelligence
Produce structured and detailed drug summaries for internal databases
Ensure content accuracy, completeness, and adherence to SOPs
Meet weekly production volume and quality KPIs
Collaboration & Process Improvement
Work closely with cross-functional and international teams across India and Spain
Participate in workflow optimization and process improvement initiatives
Adapt to evolving research processes and business requirements
Complete assigned tasks from reporting managers within specified timelines
Experience Requirements
Freshers or candidates with up to 6 months of relevant experience in life sciences research, content analysis, or healthcare analytics
Experience in clinical research documentation, scientific writing, or regulatory data review is advantageous
Educational Qualifications
M.Pharm, B.Pharm, or D.Pharm degree required
Required Skills & Competencies
Knowledge of content analysis and scientific editing
Strong written and verbal communication skills in English
Understanding of clinical trials and pharmaceutical terminology
Proficiency in Microsoft Office (Word, Excel, PowerPoint)
Strong research and analytical skills
Effective time management and ability to meet deadlines
Ability to work independently and within a collaborative team
Adaptability in fast-paced, KPI-driven environments
Basic understanding of ICH-GCP and regulatory frameworks is a plus
Preferred Qualifications
Familiarity with AI tools used in research or content workflows
Basic knowledge of SQL or Python for data handling and analysis
About the Team
The Drug Development Intelligence team analyzes clinical trials, regulatory data, company pipelines, and scientific disclosures to provide structured pharmaceutical intelligence to global stakeholders. The team operates across Hyderabad, Bengaluru, Chennai (India), and Barcelona (Spain).
This role supports global scientists, researchers, and pharmaceutical professionals seeking detailed insights into drug development programs.
Work Schedule
40 hours per week
Monday to Friday
9:00 AM to 6:00 PM IST
Hybrid work model
Why Apply?
This position offers early-career professionals the opportunity to:
Gain hands-on experience in global drug development analytics
Work with international teams in life sciences research
Develop expertise in clinical trial intelligence and pharmaceutical pipeline tracking
Build a strong foundation in healthcare data analytics and regulatory research
Keywords for Search Optimization
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