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# Senior Statistical Programmer (FSP - Permanent Homebased)

- **Company:** IQVIA
- **Location:** Copenhagen, NY, United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Management, Computer Programming, R (Programming Language), SAS (Software), Information Technology, Data Management
- **Published:** November 14, 2026
- **Apply:** https://www.healthjobsnationwide.com/node/15660983/apply-external

## About the Role

* Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, Life Sciences, or a related field.
 * Minimum 5 years of statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.
 * Strong programming experience with SAS (Base and Macro) and R.
 * Strong knowledge of CDISC standards, including SDTM, ADaM, and Pinnacle 21.
 * Proven experience supporting efficacy analyses and statistical reporting for clinical trials.
 * Experience developing and reviewing ADaM specifications and regulatory deliverables.
 * Strong understanding of clinical trial statistical methods, TLFs, and graphical outputs.
 * Experience serving as a Study Lead or Lead Programmer on global clinical studies.
 * Working knowledge of clinical trial data, including efficacy, safety, and PK/PD.

Preferred Qualifications

 * Hands-on experience with R programming in a clinical research environment.
 * Experience supporting global regulatory submissions (FDA, EMA, PMDA).
 * Previous experience working within an FSP model supporting pharmaceutical sponsors.

If you are looking to take a leading role within a collaborative FSP environment and contribute to the successful delivery of global clinical development programs, we would love to hear from you.

## Description

* Lead and contribute to statistical programming activities across Phase I-IV clinical trials.
 * Develop, validate, and maintain analysis datasets, tables, listings, figures (TLFs), and other study deliverables using SAS and R.
 * Support efficacy and safety analyses in accordance with CDISC standards and study requirements.
 * Author and review programming specifications and related documentation.
 * Perform quality control and validation of programming outputs.
 * Support regulatory submissions and ensure compliance with global regulatory standards.
 * Collaborate with Biostatistics, Data Management, and cross-functional study teams.
 * Act as a Lead Programmer or Study Lead, providing oversight and technical guidance as required.