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Submit Resume to Email At IQVIA RDS recruitment for B.Pharma,M.pharma,B.sc,M.sc Graduates

SWARNALATHA B March 9, 2022

IQVIA RDS India Pvt Ltd Walk In Interview 2022  B.Pharma/M.pharma/B.sc/M.sc for Clinical Data Management At Hyderabad/Secunderabad, Chennai, Bangalore/Bengaluru, Delhi / NCR, Mumbai (All Areas). IQVIA RDS India Pvt Ltd Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.

  • Vacancy details:
  • Post Name: Clinical Data Management
  • Qualification: B.Pharma/M.pharma/B.sc/M.sc    
  • Experienced:2 to 6 years

Job Description: IQVIA RDS India Pvt Ltd Hiring For Clinical Data Management ! 

  • Important Details :
  • Location: Hyderabad/Secunderabad, Chennai, Bangalore/Bengaluru, Delhi / NCR, Mumbai (All Areas)
  • Note:If Interested please share your updated cv at vaishnavinandkishor.kamble@iqvia.com
  • Post of date: 09/03/2022
  • Selection Process: The selection will be on the basis of Interview.

Sr. Clinical Data Co-Ordinator SR DOC

  • Serve as Data Operations Coordinator (DOC) for one or two complex global studies with fewer than 10 operations staff (excludes DE), or serve in a leadership role to a specific DM Task.
  • Manage delivery of projects through full data management study life-cycle.
  • Manage project timelines and quality; determine resource needs; identify out-of-scope work.
  • Serve as Data Operations Coordinator or Data Team Lead.
  • Perform comprehensive data management tasks including data review, writing and resolving data clarifications.
  • Perform database designer activities for technologies not requiring extensive programming.
  • Perform comprehensive quality control procedures.
  • Independently bring project solutions to the CDM team.
  • Solve issues through using the global issue escalation/communication plan.
  • Consult with Standards Group for process issues; communicate ideas for process improvement.
  • Assist in developing and implementing new technology.
  • Understand and comply with core operating procedures and working instructions.
  • Meet objectives as assigned.
  • Develop and maintain good communications and working relationships with CDM team.
  • Interact with CDM team members to negotiate timelines and responsibilities.
  • Has the potential work as DTL/LDM on Global Data Management Project

Lab Normal Reviewer

  • Reviews Study Documents such as Protocol, ALS, DARS and Laboratory Reference Range Documents
  • Coordinating with the Lead Data Manager for all discrepancies found, identifying errors in programming in the lab set ups and review and suggest changes to eCRF specification guidelines
  • Prepares the Lab Test Question for the required analytes
  • Creates Lab IDs and enter the ranges and units for each analyte as per the lab test question form for Local Lab.
  • Creates TESTLAB in database for UAT and DEV environment for testing purpose
  • Approval for new Analytes and units from Amgen as and when required
  • Performing QC on LNR entries to assure the 100% quality

Lab Data Reviewer

  • Protocol Review for lab requirements
  • Review of ALS, DARS, DMP, eCRF Completion Guidelines and coordinates with the Lead Data Manager for

all discrepancies found

  • New Lab Parameter/New Unit/Textbook Ranges Approval Process
  • Review of source document and preparing the LTQ for LNR entry.
  • SAS Checks review
  • Review of IPD checklists
  • PIG update and upload of SAS listings
  • LLR Issue Log/Communication e-Logs (lab forms)
  • Lab data review (Lab view via J-review) monthly
  • Lab Form query resolution (system to site, system to LDR, LDR to site) on daily basis.
  • Resolve and issue queries on the lab data to ensure the lab data is clean.
  • Performs Quarterly SAS Check review to ensure the quality
  • Performing Quality review for the lab process
  • Interaction with other LDRs to verify/clarify information on new data issues.
  • Attend weekly team meetings, Doc Meetings and Client meetings as when required.

UAT

  • Providing knowledge in validation tasks and performing database validation efforts to ensure delivery of

high-quality databases.

  • Accountable for overall quality and delivery of the validation effort.
  • Develop and test databases and edit specifications.
  • Meeting objectives as assigned.
  • Develop and test databases and edit specifications, this includes:

Performs UAT for Edit Checks and Database

Updates the Edit check status appropriately

  • Communicates issues for erroneous Edit Checks to the programmer within the Data Management Plan

– Communicates any documents updates or uncertainties to the Lead Data Manger within the Data

Management Plan

  • Understand and comply with core operating procedures and working instructions.
  • Develop and maintain good communications and working relationships with CDM team.
  • Communicate ideas for process improvement

About Company:

IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technology and clinical research.

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