STEM Content Analyst job opportunity at Clarivate.

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DateMore Than 30 Days Ago bot
Clarivate STEM Content Analyst
Experience: 2-years
Pattern: full-time
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loacation India - Hyderabad, India
loacation India - Hydera..........India

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 relevant   job   experience in   secondary market research,   competitive analysis etc.   M Pharm, BPharm or D Pharm degree  is mandatory Knowledge in content analysis & editing   Good interpersonal skills   and   communication skills (written and oral)   A good   team player   with the ability to work on own initiative   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?   A nalyse   drug-based references (clinical trial s, company/research institution press releases and websites, regulatory information from FDA, EMA… )   I dentify   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   d escription, Mechanisms of Action,   p roduct 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. 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.

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