Associate STEM Content Analyst

Company: Clarivate
Company: Clarivate
Location: India - Chennai
Commitment: Full time
Posted on: 2025-10-22 05:11
We are looking for an Associate STEM Content Analyst to join our Synthesis team in Chennai (India). This is an excellent opportunity to contribute to content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 8 members based across Chennai and Barcelona (Spain) and this position reports to the Chemistry Manager. We have a strong expertise in Organic Synthesis and use specialized tools to draw chemical structures. if you are a passionate of Organic Chemistry and are interesting in drug development, we would love to hear from youAbout You – experience, education, skills, and accomplishments  MsC or Bachelor degree in Organic chemistryExperience in Chemical structure drawing tools like ISISDraw, ChemDraw or BioviaDrawSolid understanding drug development processesProficient in English, both written and spokenStrong scientific and analytical skills, with attention to detailsKnowledge of classical and modern synthetic techniques (e.g., cross-coupling, asymmetric synthesis, catalysis, biosynthesis)Ability to read, interpret, and critically evaluate scientific papers and patents.Ability to work independently and within a multidisciplinary team of diverse collaboratorsGeneral computer proficiency (MS Office) and ability to quickly learn new software toolsExperience in the use of scientific databases as e Web of Science, Pubchem, Google scholar, Google patentsIt would be great if you also had . . .  Good interpersonal skillsEffective time management skillsHigh motivation with a strong work ethic and ability to thrive in a fast-paced environmentAdherence to SOP and PoliciesExperience with AI toolsWhat will you be doing in this role?Deep analysis of scientific literature (patents/articles/meeting abstracts) to create synthesis scheme information related to drugs described in the sources, following our Editorial policiesCreate or update synthesis schemes and related information for drugs in advanced phase of development in a structured waySummarize all Synthesis scheme information described in patents and articles.Adhere to Content analysis schedules and quality standardsActively participate to team activities and work towards the process improvement by raising, discussing, and resolving subject matter and production issuesCollaborate with ROW & Cross BU groups when neededProductCortellis Drug Discovery Intelligence focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical, synthetic and pharmacological data from disparate sources into a single platform. Users will benefit from the broadest, deepest, most accurate source of R&D intelligence that has been manually curated, validated, and shared using a solution built by scientists for scientists.About the Team  We are a global, high-performing synergistic team of 8 members including associate content editors, content editors and senior content specialists based across India and Barcelona (Spain).Our main goal is to analyse journals, patents and meeting abstracts to provides content to CDDI product, including synthesis schemes, synthesis schemes description, registration of reagents and intermediates and patents and articles indexation Hybrid working system (working from office and digital workplace)Hours of Work  This is a full-time permanent position, with flexible 8 working hours/day in core time of 9:00am-6:00pm (IST). Workdays - 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.
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