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Role Purpose:
HVS Production Analysts will be responsible for HVS-CTOS tasks particularly data entry/coding of procedures being done in clinical trials.

Principal Accountabilities:
o    Assess and organize clinical trial budgets for entry into cost benchmarking database.
o    Research study to find additional study information.
o    Enter background information and cost information from each investigator budget.
o    Track entry numbers for each collection.
o    Track individual entry numbers.
o    Perform various quality control checks on all data entered.
o    Escalate issues.
o    Perform functions as directed by the project lead.

Minimum Education, Experience, & Specialized Knowledge Required:
Allied medical health professionals (preferably nurses) having an excellent grasp/understanding of medical terminologies, excellent research and analytical skills.  Proficiency in Windows applications (Excel, Word, Access).

Organization Reporting and Scope:
Typically reports to: Project Lead, Manager

Additional Requirements:
      Proficient in written/oral communication skills. Possession of analytical and problem solving skills. Ability to work independently.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com