Principal Statistician

Overview

We are looking for a Senior Statistician with 5+ years of experience in RWE/HEOR, strong oncology expertise, solid epidemiology and observational study experience, proven publication support capabilities, and strong client-facing skills. SAS is required; experience with healthcare databases (claims, EMR, registries) is essential. In this role, you will be fully-utilising your technical skills, but you will also be serving as a lead biostatistician. The successful candidate willl work within a global team, using their project management and project leadership skills.  

This role is full-time and fully-remote. The successful candidate will be based in the UK, France, Spain or Germany. 

Responsibilities

The following areas of expertise will be aligned to the role...

• Statistical expertise and scientific leadership
• Leadership and people development
• Compliance, quality and governance
• Communication and influence

Qualifications

• Master's degree or PhD in a relevant field (Biostatistics, Epidemiology, HEOR, Public Health, or related discipline). • Minimum 5 years of experience in RWE and/or HEOR studies

• Strong experience in oncology

• Strong, demonstrable SAS skills • Proven experience leading observational research studies from design to delivery• Solid understanding of epidemiology, statistical methodologies, real-world data (RWD), and observational study design• Experience developing Statistical Analysis Plans (SAPs) and providing methodological guidance on study design, patient cohorts, demographics, clinical variables, and lines of therapyExperience supporting scientific publications, manuscripts, and evidence generation activities• Strong analytical skills with the ability to interpret results and communicate findings to clients and stakeholders• Experience working with secondary healthcare data sources, such as claims databases, electronic medical records (EMR/EHR), and patient registries • Experience with US healthcare databases and real-world data sources is advantageous• Knowledge of European databases such as CPRD and disease registries is advantageous• Strong client-facing and stakeholder management skills is advantageous• Demonstrated project leadership and/or project management experience is advantageous

Why Join Us

• Remote working and flexible working hours
• Career development, mentorship, and continuous learning
• Supportive, friendly, and collaborative culture

About Phastar

Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a global team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment.

We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life-changing therapies to patients faster.

Awards & Recognition

• SCRIP – Best Contract Research Organization, Specialist Provider
• Citeline – 2025 Award Winner
• Fierce CRO Awards – Recognized Industry Leader

Apply Now

Be part of a team known for technical expertise, quality, and impact. We value Excellence, Collaboration, Integrity, Innovation, and Passion—and we seek team members who embody these qualities. Apply today!

Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce. It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.

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