STEM Content Analyst

Associate STEM Content Analyst

Job Description

We are looking for an Associate 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, Pharamacology, 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

• M.Sc, Chemistry/B.Pharm/M.Pharm(Medicinal Chemistry, Pharmaceutics or Pharmacology) related degree
• Knowledge in content analysis and editing
• Ability to draw chemical molecules in drawing tools
• Strong background in drug development processes
• Proficiency in English
• Good scientific and analytical skills, with attention to details
• High ability to interpret and explain scientific data
• Ability to work independently and within a multidisciplinary team of diverse collaborators
• General computer proficiency (MS Office) and ability to quickly learn new software tools

It would be great if you also had . . .

• Good interpersonal skills
• Effective time management skills
• 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 AI tools

What will you be doing in this role?

• To select and analyse relevant drug-focused articles and/or patents
• Drawing chemical compounds of the selected drugs from the articles and patents.
• Ability to understand and interpret complex and detailed Pharma and Chemical related information from Patents/Articles
• Achieve production volume and quality targets
• Recording of performance against target
• Taking an active role within the team to ensure targets are met
• Maintain awareness of current developments in own technology areas
• Achieve and maintain consistent quality standards effective personal planning and time management
• Maintain a flexible and adaptable approach towards process change
• To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis
• To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis.
• Actively participate to team activities and work towards the process improvement by raising, discussing, and resolving subject matter and production issues
• Collaborate with ROW & Cross BU groups when needed

Product

Cortellis Drug Discovery Intelligence focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical, 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 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.