HICFA Clinical Database Programmer

University of Hawaii System Office-posted 3 months ago
$4,264 - $7,083/Yr
Full-time • Mid Level
Educational Services
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Regular, Full-Time, RCUH Non-Civil Service position with the John A. Burns School of Medicine (JABSOM), Hawai‘i Center for AIDS (HICFA), located in Honolulu, Hawai‘i. Continuation of employment is dependent upon program/operational needs, satisfactory work performance, availability of funds, and compliance with applicable Federal/State laws. The position involves independently receiving, collating, and presenting data requested by the ISCORE-RC regarding the state of multi-center clinical trials/research conducted at JABSOM, the University of Hawai‘i (UH) and from participating institutions and schools conducting such research. The role also includes providing data management and biostatistical support for HICFA, performing biostatistical data analysis for grant proposals and research studies, and serving as HICFA's primary liaison and super user of the Clinical Trials Management System, OnCore.

  • Independently receives, collates, and presents data requested by the ISCORE-RC regarding multi-center clinical trials/research.
  • Provides data management and biostatistical support for the Hawai‘i Center for AIDS (HICFA).
  • Performs biostatistical data analysis for grant proposals and research studies conducted by HICFA.
  • Serves as HICFA's primary liaison and super user of the Clinical Trials Management System, OnCore.
  • Advises investigators of data required to achieve protocol objectives.
  • Assists with HICFA's catalog of protocol and regulatory documents on the HICFA server.
  • Assists in creating and updating the HICFA website.
  • Master's Degree from an accredited college or university in Biostatistics or related field.
  • Two to four (2-4) years of progressively responsible professional experience with responsibilities for clinical biostatistics and data management.
  • Considerable working knowledge of principles, practices and techniques in computerized databases and biostatistical programs.
  • Considerable working knowledge and understanding of applicable federal and state laws, rules, regulations and theories associated with computerized databases and biostatistical programs.
  • Demonstrated ability to resolve wide ranging complex problems through creative reasoning and logic.
  • Demonstrated ability to interpret and present information and ideas clearly and accurately.
  • Demonstrated ability to establish and maintain effective working relationships.
  • Demonstrated ability to operate a personal computer and apply word processing software.
  • Demonstrated ability to provide data management oversight.
  • Demonstrated ability to perform database programming.
  • Demonstrated ability to multitask.
  • Demonstrated abilities in good writing and compositional skills.
  • Demonstrated ability to design and interpret clinical research protocol biostatistical requirements.
  • Demonstrated ability to work independently and collaboratively within a team environment.
  • At least two (2) years of biostatistical working experience in HIV, COVID, or other health-related fields.
  • At least two (2) years of experience working with Clinical Trial Management Systems (CTMS) and/or Electronic Medical Records (EMR).
  • At least two (2) years of experience working with Statistical Package for the Social Sciences (SPSS) or similar statistical analysis software.
  • Health insurance
  • Retirement plan
  • Paid time off
  • Professional development opportunities
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