Director of Statistical Programming

United StatesRemote

Responsibilities

Team Leadership : Build, mentor, and direct a high-performing statistical programming team, fostering technical excellence and overseeing their professional development.
Development, Standards, and Validation: Lead the development, validation, and review of efficient R code to support statistical analyses and deliverables.
Enforce departmental standards for programming maintenance and code integrity.
Facilitate cross-functional standards (eCRF design, DMPs).
Proven track record of producing high-quality analysis output for regulatory audiences (FDA) and internal stakeholders.

The ideal candidate possesses a proven track record, strong leadership and communication skills, and a deep expertise in clinical trials, programming, and regulatory deliverables. PRIMARY RESPONSIBILITIES:
experience supporting clinical trials in diagnostics, biotechnology, pharmaceuticals, or related industries. At least 5 years leading a team.
Advanced degree in Biostatistics, Statistics, Computer Science, or a related field.
Expert working knowledge of R for clinical trial reporting;
experience maintaining statistical packages and computing environments under version control
In-depth knowledge of CDISC standards including SDTM and ADaM
Proven record of hiring, mentoring, and developing a successful, productive team
Demonstrated ability and enthusiasm for working on cross-functional teams with members of diverse technical backgrounds
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health.

experience with NGS, genetics, and/or oncology molecular diagnostic testing a plus The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location.
Remote USA $186,400 — $233,000 USD OUR OPPORTUNITY