W skrócie
- Zadania: Prowadzenie działań programowania statystycznego w badaniach klinicznych.
- Firma: Czołowa, niezależna CRO z silnym naciskiem na rozwój pracowników.
- Benefity: Atrakcyjne wynagrodzenie, bonusy oraz możliwość pracy zdalnej lub hybrydowej.
- Pozostałe informacje: Możliwość mentorowania młodszych programistów i wpływania na najlepsze praktyki.
- Dlaczego ta praca: Dołącz do rosnącego zespołu i rozwijaj swoją karierę w dynamicznym środowisku.
- Kwalifikacje: Magisterskie wykształcenie w statystyce lub pokrewnej dziedzinie oraz 5-letnie doświadczenie.
Senior Statistical Programmer I / II | Leading CRO | Remote or Hybrid (Warsaw) | Poland | Circa 350,000-400,000 PLN | Bonus Join a highly respected, independent CRO that is experiencing significant growth and expanding its Statistical Programming team across Europe.
They are looking for talented Senior Statistical Programmers to join their growing team in Poland, offering fully remote working or a hybrid arrangement in Warsaw.
This is an excellent opportunity to join an established, successful CRO at an exciting stage of its European expansion.
Renowned for its scientific expertise, high-quality deliverables and strong client relationships, this organisation offers the stability of an established business combined with the career opportunities of a growing team.
What really sets this opportunity apart is the investment in its people.
With a strong emphasis on long-term career development, structured training and technical progression, this is an organisation focused on building careers, not simply filling positions.
You'll have the opportunity to work alongside highly experienced professionals, gain exposure to varied and complex clinical studies, and develop your expertise across both Statistical Programming and Biostatistics.
As a Senior Statistical Programmer, you'll play an important role in delivering high-quality clinical trial programming, taking ownership of projects, supporting regulatory submissions and contributing to the continued growth of the team.
You'll also have the opportunity to mentor less experienced programmers, influence best practices and develop towards future technical or leadership positions.
Key responsibilities include: Leading statistical programming activities across clinical studies, ensuring high-quality, timely deliverables.
Developing, programming and reviewing SDTM and ADa M datasets in accordance with CDISC standards.
Programming and reviewing TLGs for clinical study reports, ISS and ISE.
Performing CDISC compliance and Pinnacle 21 validation checks.
Preparing and reviewing define. xml, annotated CRFs and associated submission documentation.
Supporting regulatory submissions and ensuring programming deliverables meet regulatory requirements.
Contributing to the development and improvement of SAS macros, programming processes and standards.
Mentoring junior programmers and collaborating closely with Biostatistics, Data Management and wider clinical teams.
What we're looking for Master's degree in Statistics, Biostatistics, Mathematics, Computer Science or a related discipline.
At least 5 years' experience in clinical trial statistical programming.
Strong technical expertise in SDTM, ADa M, TLGs and CDISC standards.
Experience working within a CRO or pharmaceutical environment.
Previous experience leading programming activities or taking ownership of study deliverables.
Strong organisational skills, attention to detail and a collaborative approach.
A genuine interest in continued technical development and long-term career progression.
What's on offer Generous salary of circa 350,000-400,000 PLN plus bonus and benefits.
Fully remote working anywhere in Poland or hybrid working in Warsaw.
The opportunity to join a successful, independent CRO during an exciting period of growth.
Excellent long-term career progression, with opportunities to move into senior technical and leadership positions.
Strong investment in training, mentoring and professional development.
Opportunities to broaden your expertise across Statistical Programming and Biostatistics.
Exposure to diverse clinical studies, therapeutic areas and international clients.
A supportive, collaborative working environment where your expertise and contributions are genuinely valued.
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Senior Statistical Programmer in Katowice – pracodawca: Warman O'Brien
Warman O'Brien to doskonały pracodawca, który oferuje elastyczne warunki pracy w roli Clinical Research Associate II w dynamicznie rozwijającym się zespole badań klinicznych. Pracując w międzynarodowej firmie biotechnologicznej, będziesz miał możliwość rozwoju zawodowego oraz uczestnictwa w innowacyjnych projektach, a także korzystania z atrakcyjnych benefitów i wsparcia w zakresie równowagi między życiem zawodowym a prywatnym.
