Principal Biostatistician | Global CRO | Home Based | Spain | Permanent |

We are partnering with a leading global CRO to recruit an experienced Principal Biostatistician to join their growing biometrics team. This is an excellent opportunity for a Principal Biostatistician looking to take on a highly visible role, providing statistical leadership across complex global clinical trials while working closely with pharma and biotech clients. You will lead studies and regulatory submissions, collaborate with cross-functional teams and external stakeholders, mentor junior statisticians, and play a key role in delivering high-quality clinical development programmes.

Aunque la experiencia profesional y las cualificaciones son fundamental para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren.

This is a fully home-based position (Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary).

What you will be doing:

Lead biostatistics activities across individual studies, programmes of studies and regulatory submissions

Provide statistical leadership and oversight throughout the clinical development lifecycle

Review and approve study protocols, Statistical Analysis Plans (SAPs), clinical study reports and other key statistical deliverables

Collaborate with sponsors, project teams and regulatory agencies to ensure high-quality study delivery

Provide statistical consultancy to support proposal development, project planning and budgeting

Participate in bid defence meetings and client presentations, representing the biostatistics function





Mentor and support junior statisticians while promoting best practices across projects

Ensure all statistical deliverables are produced to the highest quality and in accordance with regulatory requirements

What you will need

MSc or PhD in Biostatistics, Statistics or a related discipline

7+ years' experience (PhD) or 9+ years' experience (MSc) within clinical biostatistics

Extensive experience supporting Phase I-IV clinical trials within a pharma or CRO environment

Strong knowledge of statistical methodologies, clinical trial design and the drug development process

Experience leading multiple studies, submissions or clinical programmes

Excellent communication and stakeholder management skills with proven leadership experience

Ability to work effectively across cross-functional and international project teams

What's in it for you:

Competitive salary and comprehensive benefits package including medical, dental, vision, pension and life insurance

Fully home-based in Poland, Spain, Romania, Bulgaria, Czech Republic or Hungary

Excellent long-term career development and progression opportunities

Structured learning and development programmes

Opportunity to work on innovative global clinical development programmes within a collaborative and supportive environment

What to do next

If this opportunity is of interest, please apply now with your CV as the organisation is looking to welcome an experienced Principal Biostatistician to the team as soon as possible. xugodme

Not what you're looking for?

Please contact Jo Fornaciari at for a confidential discussion about potential other opportunities in the UK and across Europe.

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