Fortrea is looking for a Clinical Data Scientist - R Programmer to join our team in Poland in a fully remote setup.
In this role, you will support Centralized Monitoring by configuring and maintaining systems, setting up new studies, and developing standard and bespoke monitoring functionalities. You will work closely with Data Scientists to ensure high-quality, efficient data oversight across clinical trials
Key Responsibilities
Develop and maintain R programs to support RBQM (Risk based Quality Management) for clinical trial data
Collaborate with cross-functional teams to understand and implement project-specific data needs
Provide technical expertise and support for data analysis and reporting tasks
Perform quality control and validation of outputs to ensure accuracy and consistency
Contribute to process improvements and development of programming standards using R
Qualifications
Bachelor's degree in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Data Science)
Minimum of 2 years of experience in R programming including familiarity with R packages (e.g., Tidyverse, ggplot2, survival)
Familiarity with data visualization techniques and tools in R
Experience with clinical trial data
Knowledge in Industry R packages like ADMIRAL and OAK
Strong analytical and problem-solving skills
Excellent communication and teamwork abilities
Desirable Skills
Knowledge of other open-source packages and tools
Experience with SAS software
Familiarity with CRAN, POSIT, and other open-source repositories and products
Learn more about our EEO & Accommodations request here
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com
