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

• Atleast 2 years of relevantjobexperience insecondary market research,competitive analysis etc.

  
  

• M Pharm, BPharm or D Pharm degree is mandatory

  
  

• Knowledge in content analysis & editing

  
  

• Good interpersonal skillsandcommunication skills (written and oral)

  
  

• A goodteam playerwith the ability to work on own initiative

  
  

• Adhere to SOP and Policies

  
  

• Ability to work well under challenging situations and meet deadlines

  
  

• Proficiencywith Microsoft Office products (Word, Excel, and PowerPoint)

  
  

It would be great if you also had...

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

  
  

• Knowledge of SQL/ Python 

  
  

What will you be doing in this role?

• Analysedrug-based references (clinical trials, company/research institution press releases and websites, regulatory information from FDA, EMA…)

  
  

• Identifynew drugs and/or drug updates (new drug names, development phase, target disease, formulation, organizations involved in drug development…) 

  
  

• Able tounderstand and process reference information,summarizeand edit itwithout 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

  
  

• Activelyparticipatewith 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 developmentteamanalyseclinical trials,company/research institutionpress releases, websites and pipelines andgovernmentalregulatory informationand provides content to CDDI. Content includesdetaileddescription, Mechanisms of Action,product categories, drug development status, drug activity and target diseases, regulatory information,milestonesand a detailedand structureddrug summary. External stakeholders would be scientists interested in researching the details ofdrug development for specificdiseases.The team is spread across2locations: Bengaluru,Hyderabadand Chennai inIndia; and Barcelona, Spain. 

Hours of Work 

40 hours/per day 9:00 AM to 6:00 PM IST. This is a full-time position

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.