Lead Clinical Database Analyst in San Diego, CA

$80K - $100K(Ladders Estimates)

NuVasive   •  

San Diego, CA 92101

Industry: Healthcare

  •  

Less than 5 years

Posted 65 days ago

This job is no longer available.

Job Description

Our Clinical Database Analyst is key in supporting all areas of SAS reporting and clinical database management for post-market and regulatory studies of NuVasive medical devices, procedures, systems, and related endeavors.

This will include supporting clinical study plan generation, data collection, data quality initiatives, database management, data reporting, data analysis, results interpretation, and reporting in all relevant internal and external venues.

Essential Responsibilities

  • Create and manage a SAS programming environment to generate and automate the production of tables, listings, figures, and custom reports
  • Support clinical trial data management activities to include database setup (SQL Server); case report form (CRF) and electronic data capture (EDC) data entry screen design; edit checks; query generation and tracking; audit trail monitoring; and user acceptance testing (UAT)
  • Support the creation, execution, and maintenance of clinical databases and reporting on SpineTRACK - our multicenter patient outcomes registry
  • Partner and openly communicate with the study teams to proactively address operational issues and clinical data questions, liaise with the data monitoring team to ensure accurate and timely data entry and lead efforts in data clean-up phase of studies
  • Develop and implement corporate procedures, which will include writing or revising standard operating procedures (SOPs) and work instructions (WI) regarding data management and programming processes
  • Organize and process historical data sources, in collaboration with organizational priorities and clinical scientists/medical writers
  • Demonstrate a high level of product and procedure knowledge to support the responsibilities of the role, and independently provide training on database processes as necessary
  • Must be highly-motivated, team-oriented, and organized with a strong attention to detail. Must have the ability to write documentation and understand, interact and communicate effectively with others
  • Assist research and other project team members in additional responsibilities as required

Basic Qualifications

  • B.S. in a scientific discipline
  • Three or more years of relevant work experience
  • Proven success working in a database management and SAS programming role
  • Advanced database management and SAS programming experience and proficiency
  • Solid experience in data visualization, graphing, and flow-charting
  • Familiar with and adheres to Good Clinical Practice (GCP) standards as applied to Clinical Trial Data Management

Preferred Qualifications

  • Master's degree or higher in a mathematical, computer science, or statistical field with 5+ years of experience
  • Experience in a clinical or industry setting within the medical device industry
  • Study experience focused on Spine or Orthopedics
  • Proficiency in clinical research, basic medical writing and understanding of medical terminology


Valid Through: 2019-9-11