# Senior Statistical Programmer

**Company**: IQVIA
**Location**: Frankfurt, Hesse
**Experience**: senior
**Job type**: full-time
**Category**: Data Science
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/Senior-Statistical-Programmer--FSP---Permanent-Homebased--m-w-d_R1579647?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/senior-statistical-programmer-0302d662-7d0/

## Description

We are seeking an experienced Senior Statistical Programmer with strong expertise in efficacy analysis, clinical trial reporting, and regulatory deliverables to support Phase I-IV studies.

**Key Responsibilities**

- 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.

**Required Qualifications**

- 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.

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## Skills

### Required
- SAS
- R
- CDISC standards
- SDTM
- ADaM
- Pinnacle 21
- statistical programming
- efficacy analyses
- statistical reporting
- clinical trials

### Nice to have
- R programming
- global regulatory submissions
- FSP model

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Frankfurt-Hesse-Germany/Senior-Statistical-Programmer--FSP---Permanent-Homebased--m-w-d_R1579647?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)