Associate STEM Content Analyst – Shape the Future of Drug Development
Summary:
Clarivate is seeking a highly motivated and detail-oriented Associate STEM Content Analyst to join our CDDI Drugs team in Hyderabad, India. This role offers an exceptional opportunity for recent graduates or early-career professionals with a background in pharmacy to contribute to cutting-edge research in the drug development landscape. As an integral part of our global team, you will analyze critical scientific data, identify emerging trends, and ensure the accuracy and quality of our drug intelligence databases. If you are passionate about scientific content, data analysis, and making a real impact on the future of healthcare, we encourage you to apply.
About Clarivate:
Clarivate is a global leader in providing trusted insights and analytics to accelerate the pace of innovation. We deliver critical data, information, workflow solutions, and deep domain expertise to innovators worldwide. Our mission is to help customers discover, protect, and commercialize their inventions more quickly and effectively.
Job Description:
As an Associate STEM Content Analyst, you will play a vital role in shaping the future of drug development by meticulously analyzing and curating critical scientific information. Your responsibilities will encompass a wide range of tasks, including:
Key Responsibilities:
- In-Depth Content Analysis: Scrutinize drug-based references, including clinical trial reports, regulatory documents from agencies like the FDA and EMA, and press releases from pharmaceutical companies and research institutions.
- Drug Identification and Tracking: Identify and document new drugs, their development phases (preclinical, Phase I, II, III, etc.), target diseases, formulations (tablets, injections, etc.), and the organizations involved in their research, development, and commercialization.
- Comprehensive Online Research: Conduct thorough online research to gather drug-related content and keep abreast of the latest scientific updates, emerging trends, and competitor activities.
- Content Summarization and Editing: Summarize, edit, and proofread scientific and technical content, ensuring high grammatical accuracy, conceptual clarity, and adherence to established style guidelines.
- Performance and Productivity: Meet weekly volume, quality, and key performance indicator (KPI) targets, demonstrating efficiency and a commitment to delivering high-quality data.
- Global Collaboration: Collaborate effectively with global teams located in India, Spain, and other regions, fostering a collaborative and supportive work environment.
- Process Improvement: Adapt to process improvements and workflow changes, demonstrating flexibility and a willingness to embrace new technologies and methodologies.
- Compliance: Follow all standard operating procedures (SOPs), guidelines, and compliance policies to ensure data integrity and adherence to regulatory requirements.
Qualifications:
Minimum Requirements:
- Fresh graduates or candidates with up to 6 months of relevant experience.
- Bachelor’s degree (B.Pharm), Master’s degree (M.Pharm), or Diploma in Pharmacy (D.Pharm).
- Demonstrable strength in content analysis, editing, and a solid grasp of scientific concepts, particularly in the pharmaceutical domain.
- Excellent written and verbal communication skills, with the ability to articulate complex information clearly and concisely.
- Strong time management skills, with the ability to prioritize tasks and meet deadlines in a fast-paced environment.
- Exceptional teamwork skills, with the ability to collaborate effectively with colleagues from diverse backgrounds.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
Preferred Skills:
- Knowledge of SQL or Python programming languages (a plus).
- Experience using AI tools for productivity enhancement (e.g., natural language processing, machine learning).
- Ability to thrive in fast-paced, deadline-driven environments, demonstrating resilience and adaptability.
Why Join Clarivate?
- International Exposure: Work directly with an international drug development research team, gaining valuable experience in a global context.
- Comprehensive Learning: Gain exposure to all facets of drug development, including clinical trials, regulatory research, and scientific data processing.
- Hybrid Work Environment: Enjoy a hybrid work culture with a schedule of Monday to Friday, 9 AM to 6 PM IST.
- Meaningful Contribution: Contribute directly to global databases that are used by researchers, pharmaceutical companies, and regulatory agencies worldwide.
- Career Growth: Unlock opportunities for career growth in research analytics, pharma intelligence, regulatory insights, and other specialized areas within Clarivate.
Job Location:
Hyderabad, India
Work Mode:
Hybrid, Monday–Friday
How to Apply:
If you are a motivated and enthusiastic individual with a passion for scientific research and data analysis, we encourage you to apply for this exciting opportunity.
