Senior STEM Content Analyst (Medicinal Chemistry) job opportunity at Clarivate.

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DatePosted 3 Days Ago bot
Clarivate Senior STEM Content Analyst (Medicinal Chemistry)
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Pattern: full-time
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degreeAssociate
loacation India - Chennai, India
loacation India - Chenna..........India

We are looking for a Senior STEM Content Analyst to join our CDDI Chemistry team in Chennai (India). This is an amazing opportunity to work on content analysis for our Cortellis Drug Discovery Intelligence (CDDI) product. The team consists of 17 members based across Chennai, Hyderabad, Bangalore and Barcelona (Spain) and this role reports to the Chemistry Team Manager. We have a great skill set in Chemistry, Pharmacology, Medicinal chemistry, Synthesis and complementary skill sets to address challenges in drug discovery, including new chemical drugs identification, curation of drugs and formulations. We would love to speak with you if you have an understanding of chemical drug products. About You – experience, education, skills, and accomplishments: Master's Degree in relevant Scientific or Technological subject (General Chemistry/Organic Chemistry) 5 Years of Relevant Experience in medicinal chemistry reference analysis Strong understanding of scientific chemistry literature, including patents, clinical trials, and company pipeline documents. Demonstrated expertise in core chemistry concepts, proficiency in chemical structure drawing, and the ability to independently manage and own Chemistry-related policies. It would be great if you also had . . Good interpersonal skills and Effective time management skills Experience with SQL query language  Excellent English written and verbal communication skills High motivation with a strong work ethic and ability to thrive in a fast-paced environment Adherence to SOP and Policies Experience with SQL query language What will you be doing in this role? Review the editorial work of others and provide constructive and timely feedback.   Research and resolve content discrepancies. Proactively identify issues concerning content process and other related matters and presents ideas for resolution.   Support quality improvements: evaluate quality control assessors and address knowledge gaps to ensure adherence to policy; analyze the root cause for errors and provide potential corrective and preventive actions to the identified root causes.     Draft documentation related to product workflows, identify gaps in said documentation, and recommend edits or amendments.   Investigate and assist with resolution of issues for internal and external customer.   Train and onboard new team members in the core task(s) and mentor and guide them through the process to achieve targets and quality standard.    Self-training on cross processes to support critical content delivery situation and minimize risk to customers Initiate/support projects that can enhance content and processes.  About the Team : We are a global, high-performing synergistic team of members including associate content editors, content editors and senior content editors, based across India and Barcelona (Spain). Our main goal is to analyse journals, patents and meeting abstracts to provide content to CDDI product, including details like Drug Chemical Structure, Description, Mechanisms of Action, Product Categories, Drug Phase, Developmental Stage, Therapeutic activity, and all related retrospective articles and patents reported for the drug. 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 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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