Programmer

GSK

Italia

In loco

EUR 50.000 - 70.000

Tempo pieno

5 giorni fa

Candidati tra i primi

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Vantaggi offerti da questo lavoro

Smart working 50%

Healthcare plan

Pension fund

Employee support

On-site gym

On-site canteen

Shuttle service

Nursery support

Tax assistance

Descrizione del lavoro

GSK in Siena, Italy, seeks a Programmer to design, build and validate coding solutions that turn clinical and real-world data into clear, trustworthy results. You will collaborate with statisticians, data scientists and study teams in an agile environment to deliver validated outputs and reports.

We value practical problem solving, clear communication, and experience with SAS, SDTM/ADaM, and scripting languages like R or Python. Italian and English fluency is essential.

Competenze

Degree or equivalent practical experience in a related field.
Experience programming in a regulated environment (pharma/biotech/CRO).
Experience with R or Python scripting, and data standards like SDTM/ADaM.

Mansioni

Develop, test and document code to transform and report clinical datasets.
Produce validated datasets, tables and figures meeting standards and timelines.
Support SDTM/ADaM and reporting activities throughout study lifecycle.
Review code and outputs for accuracy and reproducibility.
Collaborate with statisticians and data scientists in an agile setting.

Conoscenze

Scripting languages (R/Python)

Clear written and verbal communication

Cross-functional collaboration

Fluent Italian and English

Quality control and code reviews

CDISC SDTM/ADaM familiarity

Formazione

Degree in computer science, statistics, mathematics, life sciences, or related field

Strumenti

SAS programming

SQL

Jira

Descrizione del lavoro

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.

Find out more: Our approach to R&D

Job title

Programmer

Location

Siena, Italy

Employment type

Permanent, full time

Closing date for applications

6 September 2026

Position Summary

You will design, build and validate programming solutions that turn clinical and real‑world data into clear, trustworthy results. You will work closely with statisticians, data scientists, study teams and external partners. We value curiosity, practical problem solving and clear communication. This role offers growth in technical skills, chances to influence study decisions, and the opportunity to make meaningful contributions to our mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities

Develop, test and document code to transform, analyse and report clinical and observational datasets.
Produce validated datasets, tables, listings and figures that meet agreed standards and timelines.
Support SDTM, ADaM and reporting activities, including study and standard program development, validation and review.
Review and quality check code, outputs and documentation to ensure accuracy and reproducibility.
Collaborate with statisticians, data scientists and study teams to implement analysis plans and resolve technical questions.
Help introduce and apply improved tools, automation or coding patterns within an agile delivery setting.

Why you?

Basic Qualifications & Skills

Degree in computer science, statistics, mathematics, life sciences, or a related field, or equivalent practical experience.
Practical programming experience in a regulated environment such as pharmaceutical, biotech or a CRO.
Experience with scripting or statistical languages such as R or Python.
Familiarity with clinical data standards (for example CDISC SDTM and ADaM) or experience mapping and transforming complex datasets.
Experience producing validated outputs and performing code reviews or quality control.
Clear written and verbal communication skills for effective cross‑functional collaboration.
Fluent Italian and English, both written and spoken.

Preferred Qualifications & Skills

Hands‑on experience with SAS programming and SQL.
Experience preparing submission‑ready files and documentation such as define.xml and reviewers' guides.
Experience building automation, reusable code libraries or tools to improve efficiency.
Familiarity with data visualisation tools and exploratory analysis packages.
Understanding of regulatory expectations for clinical data deliverables.
Experience working in Agile teams and using collaboration tools such as Jira.

What we offer:

Permanent contract in a very Inclusive environment
Smart working up to 50%
Flexible Benefits
Company Healthcare Plan
Integrative pension fund
Employee Assistance Programme
Prevention services and vaccination clinic
Tax assistance
Local nursery agreement
Postal service, laundry, shoe repair and tailoring
On Site Gym
On Site canteens and coffee corners
Free company bikes and shuttle

What we value

We value people who are open, collaborative and focused on delivering quality results. We aim to create an environment where everyone can contribute and grow. You will be supported to learn new skills, adopt better ways of working and take on greater responsibility. We encourage people from all backgrounds to apply.

Please note that international relocation support cannot be provided; therefore, only candidates who are already based in the indicated country can be considered.

Skills