Lead Statistical Programmer

Posted 10 Hours Ago
Be an Early Applicant
Manila, First District NCR, National Capital Region
Senior level
Healthtech • Biotech
The Role
As a Lead Statistical Programmer, you will generate statistical programming for clinical trials, oversee activities by external vendors, review data specifications, provide statistical analysis support, and ensure the quality of datasets. You will also author related procedures and represent the biostatistics team in meetings with stakeholders.
Summary Generated by Built In

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.

Meet the team:


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:

  • 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).

  • You oversee programming activities by external vendors.

  • You provide input in developing CRF, database, data validation plan, and specifications of analysis datasets.

  • You review eCRF (EDC system) annotations and data specifications to provide input to the Data Management Team for analysis needs.

  • You check for consistency and adequacy of eCRF and database (EDC System) for analysis needs.

  • You 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.

  • You write or review analysis programs as specified in the protocol or the Statistical Analysis Plan (SAP).

  • You write or modify efficient design and code SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH, SAS/ETS, SAS/IML, and SAS MACROS.

  • You establish and monitor data transfer specifications across different data environments for ongoing trials to identify study conduct or data quality issues.

  • You review or author statistical programming-related Standard Operating Procedures or Working Instructions.

  • You participate in operations meetings, address issues, and represent the biostatistics team at meetings with cross-functional teams, contract organizations, and regulatory agencies, when necessary.

  • You assume and perform other duties as assigned.


What makes you successful:

  • You have at least 8 years of experience in statistical programming in clinical environments and the biomedical industry.

  • Your working knowledge includes template utilities such as SQL, and SAS tools like SAS Advanced, SAS Macro, and SAS SQL. You possess data conversion knowledge and skills to/from various data formats such as XML, CSV, Excel, and SAS.

  • 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.


What you’ll get:

  • A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.

  • A full and comprehensive benefits program.

  • Growth opportunities on a global scale.

  • Access to career development through in-house learning programs and/or qualified tuition reimbursement.

  • An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.

#LI-Hybrid

To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.

Top Skills

SAS
The Company
Chatswood, New South Wales
7,214 Employees
On-site Workplace
Year Founded: 1999

What We Do

Dexcom Corporation 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 over 10,000 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

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