We are looking for a STEM Content Analyst to join our Content Operations team in Hyderabad, India. This is an amazing opportunity to be a member of a talented and vibrant team.

The analyst will participate in an Editorial or Content Operations team and assist in the creation and/or acquisition, preparation and delivery of assigned content and information for creating products and product functionality in specific publication media.

About You: Experience, Education, Skills, and Accomplishments

Master’s degree in Pharmacy (MPharm or Pharm D)At least 2+ years of relevant experience in primary market research, respondent recruitment, data collection, project management, etc.Ability to communicate clearly, concisely, and objectively in written and spoken English, while ensuring timely delivery of projects to our clients.Proficiency with Microsoft Office products (Word, Excel, and PowerPoint)A flexible and collaborative approach to work, with well-developed expertise in market research methodologies.Ability to handle tight deadlines. Business acumen that supports project success, ongoing improvements, and relationships with internal and external stakeholders.Highly self-motivated and able to work independently or with a team to produce high-quality deliverables.Mature communicator, capable of handling high-profile stakeholders.

What will you be doing in this role?

To analyse drug-based references (clinical trials, company/research institution press releases and websites, regulatory information from FDA, EMA…)To 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 errorsTo do comprehensive search for finding drug related references onlineShould meet weekly production volume and quality targets consistently; achieve KPI metricsActively participate with the team and work towards process improvementCollaborate with ROW & Cross BU groups on demandTo be flexible and adaptable towards process changeTo complete the tasks demanded by your line manager / director on a permanent or temporary basis

About the Team   

Drug development team analyze 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.

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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 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.