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Associate Content Editor

0-1 years
Not Disclosed
18 June 10, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Associate Content Editor

Company: Clarivate

Team: Experimental Pharmacology & Models Team

Location: Chennai

Work Model: Hybrid

Hours of Work:

  • 40 hours per week
  • 9:00 AM to 6:00 PM IST

Product Overview:

Cortellis Drug Discovery Intelligence (CDDI) focuses exclusively on pharma and drug development, harmonizing and integrating essential biological, chemical, and pharmacological data from disparate sources into a single platform. This solution, built by scientists for scientists, offers the broadest, deepest, and most accurate source of R&D intelligence that has been manually curated, validated, and shared.

About the Team:

The Experimental Pharmacology & Models team analyzes journals, patents, and meeting abstracts to provide content for CDDI. The content includes pharmacological activity data for therapeutic drugs and experimental models that simulate human diseases. External stakeholders include scientists researching the details of specific diseases.

Position Overview:

We are looking for an Associate Content Editor to join our Experimental Pharmacology & Models team in Chennai. This is an excellent opportunity to work on CDDI within a small, talented, and creative team. This role reports to the Team Manager.

Educational Requirements:

  • M Pharm, B Pharm, or D Pharm degree

Experience Requirements:

  • 0 to 1 year experience in pharmacology content
  • Knowledge in content analysis and editing

Key Responsibilities:

  • Review, analyze, and update pharmacological activities and internal core database (CMS) according to the proposed guidelines.
  • Review, analyze, and update in vitro, in vivo, and ex vivo studies from patents, references, posters, and conferences in CMS.
  • Update pharmacological parameters and units measured, materials, and methods used in respective activities from patents, references, posters, and conferences.
  • Detail pharmacological information about drugs, including the animal model, dose regime, endpoint measurements, and duration of the drug.
  • Achieve production volume and quality targets.
  • Record performance against targets.
  • Actively participate within the team to ensure targets are met.
  • Maintain awareness of current developments in relevant technology areas.
  • Consistently achieve and maintain quality standards.
  • Plan and manage time effectively.
  • Adapt flexibly to process changes.
  • Identify and address personal technology training and developmental needs.
  • Promote personal and team safety by adhering to legal and recognized safety practices.
  • Perform any other reasonable duties as requested by the line manager or director on a permanent or temporary basis.

Additional Information:

At Clarivate, we are committed to providing equal employment opportunities for all individuals 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.

Contact:

Interested candidates are encouraged to apply through the official application process provided by Clarivate.

Note: Clarivate does not accept unsolicited resumes from recruiters or third parties. Please refrain from making phone calls or sending emails regarding this posting.