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Principal Statistical Programmer

Rad Hires
Desde casa

Postulación rápida

Detalles del empleo

Medio tiempo

Descripción completa del empleo

About Us

Rad Hires is a US-based recruiting firm specializing in connecting top Latin American talent with leading companies in the United States. We work as a strategic partner for our clients, taking the time to understand each candidate's background and goals to match them with the right opportunity.

About the Company

Our client is a well-established US biometrics consulting firm with over 30 years of industry experience, working exclusively with leading pharmaceutical and biotech companies. Their team is highly credentialed — 95% hold advanced degrees with an average of 15 years of experience. They are now building an offshore biometrics model in Latin America, and this is an opportunity to be part of that first wave.

About the Role

We are looking for a Senior Statistical Programmer to conduct programming activities for clinical trials, early phase projects, and publication activities — working directly with US pharma and biotech client teams. This is a high-impact, fully remote role for a senior professional who can hit the ground running

Key Responsibilities

Lead at least one study team, providing technical and domain-related guidance
Manage and mentor a team of 2–4 programmers as needed
Prepare SAS analysis datasets, tables, listings, and figures (TFLs) per specifications
Develop programs for graphs and tables required in CSRs, safety and efficacy reports
Validate and transform datasets and TFLs per client specifications
Support data migration from legacy datasets to CDISC or client-specific standards
Coordinate with US client teams on specifications, data issues, timelines, and reviews
Conduct all work in compliance with applicable SOPs and Quality Management Systems

Requirements

✅ Must-Haves

BS or MS in Computer Science, Statistics, Biostatistics, or related health science field
5+ years of SAS programming experience with clinical trial data
Oncology therapeutic area experience — mandatory
Strong understanding of CDISC standards (SDTM, ADaM) and regulatory requirements
Experience with CSRs, safety/efficacy reporting, and FDA submissions
Ability to work independently with minimal oversight
Strong written and verbal English — direct client interaction with US pharma teams required

✅ Nice-to-Haves

CRO or FSP environment experience
R programming knowledge
Prior experience working directly with US-based sponsors

What We Offer

Competitive USD hourly rate.
100% remote from Latin America
Work on real commercial clinical trials for top US pharma and biotech companies
Be part of the first wave of offshore biometrics talent for this client

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