Clinical Data Manager I

Roswell Park Comprehensive Cancer Center

About The Position

Coordinates data management activities for investigator-initiated clinical trials from database design through delivery to Biostatistics for analysis; interprets the study protocol and develops detailed database specifications; builds forms and calendars in the current application; ensures appropriate structure, organization, content and on-line instruction; programs on-line logic constraints to control form behavior and prevent data entry errors; maintains data collection definitions; documents data entry guidelines to facilitate consistency of data; sets up data review plans, develops data edit check routines, reviews data for missing and in-congruent data; performs patient data reconciliation between systems; utilizes a query management system to facilitate data resolution and clean-up; monitors the progress of study data; assesses for analysis milestones and releases data to Biostatistician for analysis; serves as gatekeeper for personnel access to clinical trial data; and trains all internal and external data entry personnel in database functionality and navigation capabilities. The starting salary for this position is $63,361 annually which includes a comprehensive benefits package. The listed pay range reflects the range of potential compensation for this role. The actual offer may vary based on qualifications, skills, and experience.

Requirements

  • Bachelor’s degree in a science or medical field and the equivalent of one (1) year of full-time clinical data management experience; or
  • Associate’s degree in a science or medical field and the equivalent of three (3) years of full-time clinical data management experience.
  • NOTE: Required degrees must have been granted by an accredited college or university or one recognized by Roswell Park Comprehensive Cancer Center as following acceptable educational practices.

Responsibilities

  • Coordinates data management activities for investigator-initiated clinical trials from database design through delivery to Biostatistics for analysis
  • Interprets the study protocol and develops detailed database specifications
  • Builds forms and calendars in the current application
  • Ensures appropriate structure, organization, content and on-line instruction
  • Programs on-line logic constraints to control form behavior and prevent data entry errors
  • Maintains data collection definitions
  • Documents data entry guidelines to facilitate consistency of data
  • Sets up data review plans, develops data edit check routines, reviews data for missing and in-congruent data
  • Performs patient data reconciliation between systems
  • Utilizes a query management system to facilitate data resolution and clean-up
  • Monitors the progress of study data
  • Assesses for analysis milestones and releases data to Biostatistician for analysis
  • Serves as gatekeeper for personnel access to clinical trial data
  • Trains all internal and external data entry personnel in database functionality and navigation capabilities
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