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Accenture Hiring for Medical Encoding into Clinical Data Management

Accenture is  looking for the candidates for Medical Encoding into Clinical Data Management for Hyderabad Location 
Interested candidates share your updated CV to 
Responsibilities & Authorities:

  • Efficiently reviews clinical database for investigator reported verbatim terms and assign manual codes for all the terms, which have failed to auto-encode
  • Perform manual classification of Uncoded terms within TMS using MedDRA Dictionary -and/or Client Drug Dictionary to Incorporate Coding Review Group (CRG) and WHO Peer Review (WPR) decisions from the daily/weekly annotation report
  • Participate in Coding Review Group (CRG) and/or WHO Peer Review (WPR) weekly calls to discuss on coding and query review decisions, if required
  • Correct data entry errors for paper studies, if required.
  • Draft and apply queries in TMS for the terms that cannot be classified to TMS Administrator
  • Applying internal actions or discrepancy messages for approval of by Client Medical Encoding Group (MEG) staff
  • Addressing all rejected internal actions or discrepancy messages.
  • Complete all coding activities in accordance to project timelines and milestones, like study lock, interim lock, DB lock, etc.
  • Consistently demonstrate skilled use of client software and applications like Oracle Clinical (Thesaurus Management System), J*Review, SQL
  • Effectively perform assigned duties following standard processes and procedures of the coding group.
  • Monitor workload and maintains patient database such that coding is kept current.
  • Run and review routine Consistency Report (J*Review) for relevant dictionary
  • Communicate findings from Consistency Report J*Review to Client Project Lead.
  • Perform review of uncoded terms and communicate findings to onshore team, if required
  • Generate AWARE NVTA reports and resolve conflicting mappings and send to CRG, if required.
  • MedDRA version upgrade potential manual remap identification – running SQL queries and searching dictionaries for terms to be reviewed by BMS governance for potential re-mapping, if required
  • MedDRA version upgrade impact analysis report generation – running reports and publishing once pre-activation is completed, if required
  • Demonstrate ability to work with a wide variety of people including Protocol Managers and Medical Encoding Protocol Lead in achieving program and protocol timelines.
  • Assist in writing formal procedures and working guidelines within the coding group, if required
  • Support information sharing and collaborates with Protocol Managers and coding review Committee on coding verbatim terms and assigning upper level terms as needed.
  • Bridging to each next step in the structured problem solving process
  • Coordinate team logistics.
  • Train/Support new joiners and assisting existing Coders on coding updates, conventions, process updates etc., as required
Educational Requirement:
  • Perffreble only Bachelors of Pharmacy and Masters in Pharmacy
  • Average experience – two years / relevant experience – three years
  • Medical terminology knowledge will be required.

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