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  • Full Time
  • India
  • Posted 6 days ago
Purpose of the role
This role assumes an individual contributor responsibility for source document curation of clinical and structure activity relationship data from relevant literature available in patents/journals/client documents as per database updation/ project requirements.
Designation Curator
Grade and Level A1/A2
Role type (Primary level of contribution) Individual Contributor
Business Unit (P&L) Informatics
Job Function GOSTAR
Job Family (Specific sub-function) Data Curation
Location (City name) Hyderabad - IDA Uppal, Plot No.6, Survey No.1
Job Responsibilities

Data Curation:

  • Clearly understanding curation protocol/ specifications from Supervisor
  • Check for source document in web search engines to capture clinical data.
  • Search for synonyms of the compound online and in source documents to capture synonyms in internal tool
  • Check the assigned task for duplicity
  • Check for source document availability and coordinate with library manager to acquire source documents
  • Capture the following data from the document in specified format on internal tool:
    • For clinical candidate database or drug database assignments: Phase details, target, drug development history, reference data, structure details, assay data, metabolism DCM, assay data, clinical data and any other data as specified by client
    • For Mechanism based toxicity studies: Reference data, Assay data, Activity data, Structure details, Metabolism MBT, Metabolism DCM, Toxicity MBT, Toxicity structure
    • For Updates: Reference details, Assay details, Activity details, Structure details, Core group details
  • For Updates: Assess need for review process and update internal tool accordingly
  • Submit data for review on online tool
  • Correct errors identified by Review Analyst or Supervisor during review
  • Complete rework of tasks rejected by Review Analyst/ Supervisor in given timeframe with desired accuracy

Data Excerption:

Support Project Manager in data excerption process by performing zero records check

Vocabulary Management:

Identify new standard values during curation, cross validate with deposited controlled vocabularies in Scribase/ DCM tools and coordinate with vocabulary manager for master record generation


Enhance scientific subject matter expertise (onchemical structures, metabolism, clinical trials, Structure activity relationships etc.), knowledge of internal tools and productivity, through regular domain trainings/ tool trainings/ one on one trainings with supervisor

Relationships around the role
Reporting to (Business) Project Manager (GOSTAR)
Reporting to (Matrix) NA
No of Reportees Direct: 0, Indirect: 0
Key External Stakeholder(s) Client
Key Internal Stakeholder(s) IT Support Team, Database Team
Competencies critical for the role
Scientific/ Technical
Competencies Proficiency level
1. Knowledge of Chemistry Basic
2. Knowledge of related Scientific Databases Basic
3. Knowledge of Biology Basic
4. Knowledgeof Drug Development Process Basic
5. Knowledge of Clinical Trial Process and Databases Basic
6. Knowledge of relevant software (e.g. Chemdraw, ISIS/ Symyx Base, ISIS/ Symyx draw, Marvin Sketch) Basic
To be updated  
Academic qualifications and experience required for the role
Educational Qualifications M.Sc. (Microbiology, BIO Technology, Bio Chemistry)
Relevant experience 1 - 4 years
Additional Requirements NA
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