Director, Biostatistics

Pfizer Inc.; Knaphill; On-site; GBP 140,000 - 180,000; Full time

Job summary

Pfizer Inc. is seeking a Director of Global Development to lead statistical strategy across inflammation, immunology and specialty care programs. You will shape study design, analysis plans, and data interpretation while coordinating global teams.

The role requires a Master's or PhD in Statistics/Biostatistics with extensive clinical trial experience, and strong programming skills in R, SAS or Python. You will partner with Clinical, Regulatory and Commercial units to drive timely,

Qualifications

• Master's or PhD in Statistics/Biostatistics with extensive clinical trial experience.
• Experience applying statistics to clinical trials and leading cross-functional teams.
• Excellent verbal and written communication skills for collaboration.
• Proficiency in R, SAS, or Python and reproducible research workflows.

Responsibilities

• Provide scientifically rigorous statistical leadership for study designs, analysis plans, and regulatory submissions.
• Ensure quality and timeliness of statistical deliverables, ensuring regulatory compliance.
• Collaborate effectively with clinical teams, regulatory bodies and cross-functional partners.

Skills

Statistical Leadership

Clinical Trials Experience

Communication Skills

Cross-functional Collaboration

Education

Masters or PhD in Statistics/Biostatistics

Tools

R

SAS

Python

Job description

and external organizations to drive project success. Innovate: Participate in research on innovative statistical methodologies that align with Pfizer's business needs.

What We're Looking For

• Educational Background: A Master's or PhD in Statistics/Biostatistics (or a related field) with extensive clinical trial experience.
• Strong Statistical Skills: Proven ability to apply statistical methods to clinical trials and provide leadership to cross-functional teams.
• Communication Skills: Excellent verbal and written communication skills to collaborate effectively with colleagues.
• Technical Proficiency: Experience with statistical programming languages (R, SAS, or Python) and reproducible research tools.

Working Conditions

This role may involve managing contract biostatisticians and requires a commitment to staying informed on advancements in statistics. You will interact with various departments, including Clinical, Regulatory, and Commercial teams, ensuring a collaborative environment.

Why Join Us?

At Pfizer, we believe in:

• Flexibility: We foster a trusting workplace culture that promotes work-life harmony, allowing you to be your best self.
• Growth Opportunities: Engage in a culture of continuous learning and innovation, where your contributions can lead to meaningful outcomes.
• Diversity and Inclusion: We celebrate a diverse workforce, ensuring that everyone feels empowered and supported.
• Disability Confidence: We are committed to making reasonable adjustments to support your application and career journey.

Application Deadline

The closing date for applications is September 24th. Please ensure you have the relevant authorization to live and work in the UK.

Our Purpose

Breakthroughs that change patients' lives... At Pfizer, we are guided by our values of courage, joy, equity, and excellence. Join us in our dedication to transforming millions of lives through our innovative digital transformation strategy, enhancing health outcomes and patient experiences.

Your journey with Pfizer starts here! Let's start the conversation and explore how you can contribute to our mission.

Job Description

Join Our Team as a Director of Global Development! Are you ready to make a significant impact in the world of healthcare? At Pfizer, we are on a mission to transform patients' lives through innovative solutions in Inflammation, Immunology, and Specialty Care. As a Director, you will play a pivotal role in planning, directing, and coordinating complex global development projects. Your expertise will guide clinical design, trial conduct, data management, and regulatory submissions, all while fostering collaboration across various teams.

Your Responsibilities

• Provide Statistical Leadership: Offer scientifically rigorous statistical input into study designs, analysis plans, and regulatory submissions.
• Ensure Quality and Timeliness: Be accountable for the quality and timeliness of statistical deliverables, ensuring compliance with regulatory requirements.
• Collaborate Effectively: Build strong partnerships with clinical teams, regulatory bodies