As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and therapeutic areas, or choose to focus your career on working with a specific sponsor and gaining in depth knowledge of a specific therapeutic area and compound.
You will become a part of a team with an inherent breadth of knowledge and expertise in small, single center Investigator studies to multi-site, multi-national trials in Phases I to IV of clinical development, as well as observational studies. From initial planning meetings at the study design stage through to implementation and execution, our team of skilled statistical programmers will employ industry-accepted statistical tools and techniques, as well as innovative consulting, to provide the quality and efficiency of projects.
Parexel develops and delivers cost effective, high-quality training programs for those employees that are directly involved with sponsor functional partnerships to ensure that our statistical programmers can quickly step in to make significant contributions to the success of a study. In addition, you will receive the opportunity to shape your development through quarterly conversations with your manager.
- Full Time
- Travel: Minimal
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Check out the top traits we’re looking for and see if you have the right mix.
- Team player
"I have learned a great deal and developed my expertise. The management team here is open and honest and it is refreshing to be treated with a high degree of trust and flexibility. I have been fortunate to work on a wide variety of projects and partnerships and the work is always interesting."Richard – Principal Statistical Programmer
We are one truly global team working together to propel each client´s journey ahead faster.
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Opportunity to learn and grow through a performance and development goal-setting program.
Work with industry leaders and subject matter experts.
Opportunity to work on a wide range of therapeutic areas and medical devices.
As a Statistical Programmer you will support various SAS® programming activities related to the analysis and reporting of clinical study data; you will use programming techniques to produce analysis datasets, tables, figures and data listings ensuring first-time quality, traceability and regulatory compliance.
- Improve/develop your SAS® programming skills and broaden knowledge of clinical trial industry.
- Participate in preparation of electronic submission packages according to the industry standards.
- Support response to regulatory agency questions.
- Prepare input to publications and conference materials.
- Develop statistical knowledge using 4GL and different SAS® procedures.
QualificationsSkills and Experience:
- Knowledge of SAS® software and experience in 4GL language.
- Understanding the principles of statistics.
- Attention to detail with a focus on quality.
- MSc/PhD degree in statistics, econometrics, mathematics, informatics or a related field or equivalent professional experience.
- Experience in Clinical Research will be an asset.
Highly qualified and dynamic team of 63 programmers in Poland. Multinational working environment. Smooth induction and training program with a dedicated mentor for candidates with no industry experience.
Flexible working hours and a friendly and supportive working atmosphere. We cooperate within projects, help each other and achieve results as a one team. We compete in running, riding a bike and burning calories!
Benefit package that includes: private medical care at LUX MED, life assurance, Cafeteria system and more!
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