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Data Analyst III

1 week ago

Manila, National Capital Region, Philippines Dexcom Full time

About Dexcom

Dexcom is a pioneering company in the field of continuous glucose monitoring (CGM). We have been at the forefront of innovation for over 25 years, driven by our mission to improve human health. Our commitment to empowering people to take control of their health has led us to broaden our vision beyond diabetes to tackle important health challenges.

We are a global leader in consumer health technology and serious health conditions. Our future ambition is to become a leading force in developing solutions for complex health issues. To achieve this, we constantly reinvent unique biosensing-technology experiences that make a significant impact on people's lives.

Job Description:

The Senior Statistical Programmer III will play a crucial role in the design, development, modification, and evaluation of technical infrastructure to accelerate clinical trials and basic research. The incumbent will perform statistical analysis and develop tracking systems to determine the efficiency of clinical trials, ensuring data quality and accuracy.

Responsibilities:

  • Generate statistical programming for all clinical trials, including data validations, statistical analysis, and report generation.
  • Oversee programming activities by external vendors.
  • Develop CRF, database, data validation plan, and specifications of analysis datasets.
  • Review eCRF annotations and data specifications to provide input to the Data Management Team for analysis needs.
  • Ensure consistency and adequacy of eCRF and database for analysis needs.
  • Provide support to the Data Management Team with their data validation plan or data management plan in later stages of product development or post-market studies.
  • Write or review analysis programs as specified in the protocol or the Statistical Analysis Plan (SAP).
  • Establish and monitor data transfer specifications across different data environments for ongoing trials to identify study conduct or data quality issues.
  • Review or author statistical programming-related Standard Operating Procedures or Working Instructions.
  • Participate in operations meetings, address issues, and represent the biostatistics team at meetings with cross-functional teams, contract organizations, and regulatory agencies when necessary.