Principal Statistician

Warman O'Brien; Stuttgart; Remote; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

Join a forward-thinking global CRO as a Principal Statistician, where you'll have the chance to work on impactful clinical trials. This fully remote role offers an excellent opportunity to leverage your expertise in biostatistics while collaborating with top-tier pharmaceutical and biotech companies. You'll be responsible for producing high-quality statistical outputs and leading junior statisticians, all while benefiting from a supportive work environment that values employee engagement and work-life balance. With structured training and a commitment to your professional growth, this position is perfect for those looking to advance their careers in a dynamic field.

Leistungen

Competitive salary and benefits package

Structured training and development plans

Condensed hours for a shorter workweek

Fully remote role available

Qualifikationen

• PhD or MSc in Biostatistics or related discipline is required.
• Experience in the pharmaceutical industry and clinical trial design is essential.

Aufgaben

• Produce and validate complex statistical outputs for clinical trials.
• Oversee junior leads and support regulatory interactions.

Kenntnisse

Biostatistics

Statistical Analysis

Clinical Trials

GCP Familiarity

Ausbildung

PhD in Biostatistics

MSc in Statistics

Jobbeschreibung

Principal Statistician | Global CRO | Germany | Home Based

Award-winning global biometric CRO has multiple opportunities for experienced Principal Statisticians to join its growing team.

Partnering with top pharma, biotech, and medical device companies, they deliver high-quality biostatistics, programming, data management, and data science services. Principal Statisticians can take on either a hands-on technical role or focus more on being a Lead Statistician. This is a great opportunity to grow with a recognized CRO, gain pharma experience, and benefit from continuous learning and development.

What you will be doing:

You will work as a statistician on clinical trials, producing and validating complex outputs of excellent quality while adhering to deliverable timelines.

You will be responsible for the statistical aspects of reporting study results. As a lead statistician across multiple studies, you may oversee junior leads and support regulatory interactions. Cardiology experience is a plus.

What you will need:

• Educated to PhD or MSc in Biostatistics, Statistics, or a related discipline
• Experience within the pharmaceutical industry with a good understanding of clinical trial issues, design, and implementation
• Familiarity with GCP and regulatory requirements
• Experience in writing SAPs and protocols

What’s in it for you:

• Recognized as an outstanding workplace, committed to employee engagement, satisfaction, and work-life balance
• Structured training and development plans in a supportive, friendly environment
• Condensed hours for a shorter workweek
• Competitive salary and benefits package
• Fully remote role available in Germany

What to do next:

If interested, please apply now with your CV, as the organization is looking to onboard Principal Statisticians as soon as possible.

Not what you’re looking for?

Please contact Mark O'Brien at [e-mail] for a confidential discussion about other opportunities in Germany and across Europe.