Clinical Data Analyst, Sarah Cannon Research Institute - Nashville, TN
Sarah Cannon Research Institute -Nashville - Nashville, TN

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GENERAL SUMMARY OF DUTIES - This position is responsible for clinical data management of SCRI clinical trials. This includes all data management activities from protocol review to the final data deliverable to the sponsor. The Clinical Data Analyst supports data management project activities according to pre-defined timelines and ensures timely completion of those projects. This position must clearly demonstrate the ability to manage multiple projects with different sponsors and timeline demands.

  • Develops and executes Data Management Plans for multiple protocols simultaneously
  • Collaborates with clinical project manager to determine study timelines and milestones
  • Participates in project team meetings to report data management status
  • Supports database design, development and testing through close collaboration with clinical programmers
  • Ensures quality standards are met for patient data in clinical database through data cleaning processes and data audits
  • Case Report Form/Data Clarification Form flow management and tracking
  • Conducts data cleaning processes according to internal SOPs and WPGs
  • Facilitates communication of data management issues to project team
  • Orchestrates ongoing data entry of clinical trial data
  • Maintains project documentation relevant to data management activities
  • Keeps management abreast of issues and progress on all assigned projects
  • Identifies and resolves any project specific data handling and data management issues
  • Responsible for ensuring the integrity of data and providing recommendations for corrective action when necessary
  • Mentors and coaches new and/or junior data management staff
  • Contributes to internal process development and improvement
  • Other duties as assigned

KNOWLEDGE, SKILLS & ABILITIES – This position requires the following minimal requirements:

  • Ability to manage multiple protocols and participate on multiple project teams simultaneously
  • Strong attention to detail
  • Excellent communication skills, oral, written and presentation
  • Excellent organizational skills
  • Excellent problem solving skills

  • Qualified candidates will have a BA/BS or equivalent experience

  • Clinical Trial experience in data management or trial management preferred or equivalent experience.

HCA Inc - 2 years ago - save job