Added
8 days ago
Type
Full time
Salary
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Related skills

r python statistics git sas

📋 Description

  • Independently strategize and develop the statistical approach for complex clinical protocols
  • Serve as the final internal statistical authority for design decisions across owned studies and
  • Serve on Data Monitoring Committees (DMCs, DSMBs) as the unblinded sponsor statistician
  • Set the vision and direction for Statistical Analysis Plans (SAPs) and mock Tables, Listings, and
  • Review and approve SAPs and mock TLFs authored by others against those standards, balancing
  • Set the vision and direction for the analysis of clinical trial data, selecting and championing the

🎯 Requirements

  • Master's (MS) or Ph.D. in Biostatistics or Statistics
  • Minimum of 9 years of experience with an MS, or 6 years with a Ph.D.
  • Minimum of 5 years of clinical trial experience required
  • Minimum of 5 years of medical device experience required; surgical and robotic-assisted device
  • Track record of developing and applying industry-leading, innovative, and integrative
  • Depth expected across several of: adaptive and group-sequential designs, Bayesian methods, use of

🚚 Relocation support

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