Associate STEM Content Analyst

We are looking for an Analyst to join our CDDI Drugs team in Hyderabad, India. This is an amazing opportunity to work on drug development research (including both primary and secondary research), competitive analysis, company communications, presentations, pipeline and clinical trial analysis, financial analysis, and produce comprehensive drug development data. The team consists of around 6 colleagues spread across India and Spain, reporting to the same team manager. We have a great skill set in the drug development industry, from drug’s patents to market access, and we would love to speak with you if you have skills or interest for the same.  

About You – experience, education, skills, and accomplishments   

• Freshers or 6 months of relevant experience in
• M Pharm, BPharm or D Pharm degree
• Knowledge in content analysis & editing
• Good interpersonal skills and communication skills (written and oral)
• A good teamplayer with the ability to work on own initiative
• Effective time management
• Highly motivated with a strong work ethic and ability to thrive in a fast-paced environment
• Adhere to SOP and Policies
• Ability to work well under challenging situations and meet deadlines
• Proficiency with Microsoft Office products (Word, Excel, and PowerPoint)

It would be great if you also had . . .   

• Proficiency in using AI tools in your day-to-day work

• Knowledge of SQL/ Python 

 What will you be doing in this role?

• Analyse drug-based references (clinical trials, company/research institution press releases and websites, regulatory information from FDA, EMA…)
• Identify new drugs and/or drug updates (new drug names, development phase, target disease, formulation, organizations involved in drug development…)
• Able to understand and process reference information, summarize and edit it without grammatical and conceptual errors
• To do comprehensive search for finding drug related references online
• Should meet weekly production volume and quality targets consistently; achieve KPI metrics
• Actively participate with the team and work towards process improvement
• Collaborate with ROW & Cross BU groups on demand
• To be flexible and adaptable towards process change
• To complete the tasks demanded by your line manager / director on a permanent or temporary basis.

About the Team  

Drug development team analyse clinical trials, company/research institution press releases, websites and pipelines and governmental regulatory information and provides content to CDDI. Content includes detailed description, Mechanisms of Action, product categories, drug development status, drug activity and target diseases, regulatory information, milestones and a detailed and structured drug summary. External stakeholders would be scientists interested in researching the details of drug development for specific diseases. The team is spread across 2 locations: Bengaluru, Hyderabad and Chennai in India; and Barcelona, Spain. 

Hours of Work 

40 hours/per day 9:00 AM to 6:00 PM IST.

Work Mode: Monday to Friday (Hybrid)

At Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.