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Clarivate Analytics

Associate STEM Content Analyst

Job Posted 22 Days Ago Reposted 22 Days Ago
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2 Locations
Entry level
2 Locations
Entry level
The Associate STEM Content Analyst will review and analyze pharmacology content, update databases, maintain quality standards, and handle technology training needs.
The summary above was generated by AI

We are looking for an Associate Content Editor to join our Experimental Pharmacology & Models team in Chennai. This is an amazing opportunity to work on Cortellis Drug Discovery Intelligence (CDDI). This is a small talented creative team and reporting to the Team Manager. We have a great skill set in Life Sciences and we would love to speak with you if you are interested in a stimulating growth-oriented position and a challenging career.

About You –

  • M Pharm, B. Pharm Graduates.
  • 0 to 2 years experience in pharmacology content
  • Knowledge in content analysis & editing

What will you be doing in this role? 

  • To review/analyze and update the Pharmacological Activities and to update the internal core database (CMS) according to the guidelines proposed.
  • To review/analyze and update IN VITRO, IN VIVO and EX VIVO study from patents, references, posters, and conferences in CMS
  • Pharmacological parameters and units measured, materials and the methods used in the respective activities from patents, references, posters, and conferences
  • Pharmacological details of the drug including the animal model, dose regime, end point measurements and duration of the drug
  • 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 make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices
  • To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis.

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 be benefited by using 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   

Experimental Pharmacology & Models team analyze journals, patents and meeting abstracts and provides content to CDDI. Content includes pharmacological activity data for therapeutic drugs and experimental models in which a human disease is modelled, looking for a treatment. External stakeholders would be scientists interested in researching the details of specific diseases.

Hours of Work  

40 hours/per day 9:00 AM to 6:00 PM IST. This is a full-time position

Location- Chennai

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.

Top Skills

Cms

Clarivate Analytics Chennai, Tamil Nadu, IND Office

No.148, Acropolis, CIT Colony Dr. Radhakrishnan Salai, Mylapore , Chennai, Tamil Nadu, India, 600004

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