Senior Biostatistician Ii

Vor 5 Tagen

Frankfurt am Main, Deutschland Icon plc Vollzeit

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.

That’s our vision. We’re driven by it. And we need talented people who share it.

If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

As a Senior Biostatistician II, you will be joining ICON’s Early Phase Data Services team allowing you to work on interesting, innovative and global clinical trials studies across a variety of different therapeutic areas. Thanks to our development and mentoring opportunities, you will be able to progress your long-term career in the direction you choose.

Locations:

- Europe (home-based OR office-based)
- United Kingdom (home-based OR office-based)

Key responsibilities:

- Acting as a Project Biostatistician / Project Manager for projects across different TA’s, Oncology TA would be an advantage
- Being responsible for all statistical aspects of multiple projects, including experimental design, analysis, and presentation of data
- Preparation and writing of SAP’s including the definition of derived data, and the design of statistical TLF’s for clinical summary reports
- Writing of the statistical methods sections of integrated study reports
- Managing statistical projects for high quality, within budget, and on-time completion
- Participating in presentations at client and investigator meetings
- Providing appropriate statistical input for regulatory submissions and responding to statistical questions raised by regulatory agencies
- Assisting in the preparation of biostatistics input to ICON research proposals
- Ongoing coaching and mentorship of team members

To be successful, you will need:

- MSc or PhD in Statistics, Biostatistics, or related field
- Min. 5 years of relevant experience in the pharmaceutical industry or related field and experience leading a regulatory submission
- In-depth knowledge of study designs, and statistical analysis in one or more therapeutic areas.
- Excellent knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages
- SAS knowledge is required

Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Are you a current ICON Employee? Please click here to apply:
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