R Developer - Clinical Data (100% remote)

23.5k - 26.9k PLN23 520 - 26 880 PLN/ mies./ mies.B2BB2B (netto)

SeniorZdalnie·WarszawaFull-time·B2B

#463459·Dodano 22 dni temu·8

Źródło: nofluffjobs.com

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Tech Stack / Keywords

RData analysisData structuresQuality controlGitAutomated testing

Podsumowanie oferty

As an experienced R Developer, you will build reliable analytical solutions and automate reporting for a global pharmaceutical project developing a unified Risk-Based Quality Management (RBQM) ecosystem. The role combines R development, clinical trial data, statistical monitoring and QTL reporting.

Wymagania

Strong commercial experience in R development and the ability to deliver solutions independently.
Very good knowledge of R, including writing clean, modular and reusable code for data analysis and reporting.
Experience with clinical trial data gained in a pharmaceutical, biotechnology or CRO environment.
Knowledge of CDISC SDTM and an understanding of clinical data structures and standards.
Experience with Quality Tolerance Limits (QTL) or statistical monitoring in risk-based quality management.
Understanding of clinical trial quality and risk concepts, including adverse events, serious adverse events and protocol deviations.
Experience in data validation and quality control with strong attention to accuracy and reproducibility.
Ability to work independently in a complex, international and cross-functional environment.
Good command of English enabling effective collaboration and technical communication.

Nice to have:

Knowledge of Git, automated testing or reproducible reporting tools.

Obowiązki

Develop and maintain R-based analytical solutions supporting the integrated RBQM ecosystem and statistical data monitoring.
Create and enhance QTL reports, including QTL determination, target, SSLL and non-statistical reports.
Configure study-specific QTL logic, including threshold limits, exposure periods, data paths and other study-level adjustments.
Work with clinical trial data and support data structures based on CDISC standards, particularly SDTM.
Automate data processing and reporting workflows to improve consistency, traceability and efficiency.
Perform quality checks and report verification covering calculation logic, parameter names and units, exposure dates, study categories, threshold reference lines, plots and summary outputs.
Collaborate with cross-functional stakeholders from clinical operations, statistics, data management, quality and technology teams.
Document code and analytical logic and contribute to maintainable, reliable and audit-ready solutions.

Benefity

Dedicated agent support for project continuity, client communication, day-to-day administration and long-term professional development.
Access to Darize Learning & Development, including webinars, industry reports and articles, learning platforms such as DataCamp and Coursera, and invitations to technical, business and lifestyle events.
Community and networking events, including Kick-Off trips, Christmas celebrations, Summer Sport Games, family picnics and cultural events.
Personalized professional development support through the Consultant Development Program, with experienced mentors and development advisors.
Private healthcare, life insurance, a sports card for you and your family members, and access to employee discounts in Poland and abroad.
E-learning platforms.
Training budget.
Integration events.
Employee Referral Program.
Language classes.
Career counseling program.
Lunch card.

Spotkania integracyjne

Kursy językowe

Opieka zdrowotna

Ubezpieczenie

Karta sportowa

Dofinansowanie szkoleń

Darize

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