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  • Full Time
  • India
  • Posted 6 days ago
Purpose of the role
This role is responsible for accurately gathering and recording clinical trial related data from patents/journals/client documents inclient specified format meeting individual productivity and accuracy targets.
Designation Analyst / Curator
Grade and Level A1/A2/A3/B1
Role type (Primary level of contribution) Individual Contributor
Business Unit (P&L) Informatics
Job Function Clinical Pharmacology
Job Family (Specific sub-function) Data Curation
Location (City name) Hyderabad - IDA Uppal, Plot No.6, Survey No.1
Job Responsibilities

Data Curation:

  • Collect task and all related files from the central location once it is allocated by project manager
  • Go through the project/ requirement abstract and extract available data in standard/ required template
  • In case of non-availability of data, flag the same in task master and request project manager for assigning new task
  • Check the assigned task for any duplicity
  • Send data related queries to the project manager for seeking resolution
  • Clarify data related queries from senior team members to improve quality of deliverable
  • Extractcurated date from full text publication/ journals/ literature to the client approved template
  • Actively curate exiting assays as needed, work closely with scientists and support them throughout the curation and validation processes.
  • Work closely with all the stakeholders to support the client's informatics initiatives and meeting their scientist's needs

Literature/data Management:

  • Gather and record clinical trial related data from external sources (PUBMED, EMBASE, COCHRANE, and Clinicaltrials.gov etc.) in specified format
  • Coordinate the transfer of raw and analyzed data to data repositories
  • Help maintain, support and document shared tools, code base and data sets
  • Save the procured literature in designated copyrighted location with restricted access

Change Management:

  • Reviewing the extracted data and correcting errors in case of any changes in the data on account of errors or client inputs.
  • Actively contribute to process improvement through optimization, innovation and new ideas

Self-Development:

  • Constantly strive to improve and develop both technical and behavioral skills through trainings and feedback discussion with manager
  • Enhance scientific subject matter expertise (On clinical trials, pharmacology), 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 - Clinical Pharmacology
Reporting to (Matrix) NA
No. of Reportees Direct: 0, Indirect: 0
Key External Stakeholder(s) Client
Key Internal Stakeholder(s) IT Support Team
Competencies critical for the role
Scientific/ Technical
Competencies Proficiency level
1. Knowledge of Drug Development Process Basic
2. Knowledge of Clinical Trial Process and Databases Basic
3. Knowledge of Pharmacology Strong
4. Knowledge of data sources (e.g. NCBI, PUBMED, EMBASE, COCHRANE, FDA, EMEA) Basic
5. Knowledge of Ontologies Basic
Behavioral
To be updated  
Academic qualifications and experience required for the role
Educational Qualifications M. Pharma (Pharmacology/Pharmaceutics/Hospital Pharmacy)
Relevant experience 0 - 2 years
Additional Requirements NA
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