Senior Statistical Programmer III

5 days ago

Manila, National Capital Region, Philippines Dexcom Full time

The Company

Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.

We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.

Summary:

Performs the design, development, modification and evaluation of technical infrastructure to expedite conduct and evaluation of clinical trials and basic research. Performs statistical analysis and develops tracking systems to determine the efficiency of clinical trials. Evaluates databases and statistical analysis programs and interacts with computer groups to determine hardware/software compatibility. Maintains expertise in state-of-the-art data manipulation and statistical analyses.

Where you come in:

  1. You will generate statistical programming for all clinical trials, including but not limited to data validations, statistical analysis, and report generation (to create tables, figures, and listings).
  2. You will oversee programming activities by external vendors.
  3. You will provide input in developing CRF, database, data validation plan, and specifications of analysis datasets.
  4. You will review eCRF (EDC system) annotations and data specifications to provide input to the Data Management Team for analysis needs.
  5. You will check for consistency and adequacy of eCRF and database (EDC System) for analysis needs.
  6. You will 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.
  7. You will write or review analysis programs as specified in the protocol or the Statistical Analysis Plan (SAP).
  8. You will write or modify efficient design and code SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH, SAS/ETS, SAS/IML, and SAS MACROS.
  9. You will establish and monitor data transfer specifications across different data environments for ongoing trials to identify study conduct or data quality issues.
  10. You will review or author statistical programming-related Standard Operating Procedures or Working Instructions.
  11. You will participate in operations meetings, address issues, and represent the biostatistics team at meetings with cross-functional teams, contract organizations, and regulatory agencies, when necessary.
  12. You will assume and perform other duties as assigned.

What makes you successful:

  1. You have at least 5 years of experience in statistical programming in clinical environments and the biomedical industry.
  2. Your working knowledge includes template utilities such as SQL, and SAS tools like SAS Advance, SAS Macro, and SAS SQL. You possess data conversion knowledge and skills to/from various data formats such as XML, CSV, Excel, and SAS.
  3. Your knowledge in R, Python, MatLab, or any other computer language skill is highly valued. You are able to work with minimal oversight and function effectively as a member of a project team.

Experience and Education Requirements:

  1. You typically require a Bachelor's degree in a technical discipline, and a minimum of 5-8 years related experience, or a Master's degree and 2-5 years equivalent industry experience, or a PhD and 0-2 years experience.

What you'll get:

  1. A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
  2. A full and comprehensive benefits program.
  3. Growth opportunities on a global scale.
  4. Access to career development through in-house learning programs and/or qualified tuition reimbursement.
  5. An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.

#LI-Hybrid

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