At a Glance
- Tasks: Design and analyse clinical trials, providing statistical expertise for drug development.
- Company: Join Pfizer, a leader in healthcare and an inclusive employer.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on diversity and inclusion.
- Why this job: Make a real impact on healthcare by supporting innovative drug development.
- Qualifications: Experience in statistics and strong communication skills required.
The predicted salary is between 63000 - 77000 £ per year.
This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.
JOB SUMMARY
Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.
Provide scientifically rigorous statistical expertise on:
- Projects and protocols in support of clinical development and for publication, presentation, access negotiation, and other evidence generation efforts for Pfizer products;
- Regulatory and Health Technology Assessment (HTA) submissions;
- Projects to maximize the value of aggregate clinical and real world data in support of drug development and other scientific strategies.
Provide study and other project level statistical counsel and communicate resource needs to teams.
JOB RESPONSIBILITIES
Provide scientifically rigorous statistical expertise on study design, statistical analysis plans, interpretation and communication of statistical results, project development plans, regulatory issues, and scientific and other product support projects.
Provide planning, delivery, and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results, support for publication activities, scientific presentations, and support to product defense.
Accountable for study or project level and submission level statistical deliverables on assigned projects.
Accountable for implementation of quality, productivity, and other best practices.
Develop effective collaborations internally and externally including, but not limited to, clinical teams, partner lines, regulatory, payer, industry, professional and academic organizations.
Ensure all study and project level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards.
Maintain compliance with all required training.
Provide statistical input and leadership to cross-functional activities, in collaboration with other statisticians, study managers, and programming colleagues, for assigned studies or regulatory and HTA submissions.
Provide to Statistics Group Lead and/or Head, Statistics input for planning support for assigned projects, studies, and submissions.
Ensure timeliness and quality of statistical deliverables according to project plans for assigned studies and projects.
Comply with all statistics and quality processes, Pfizer data standards that are applicable to statistical outputs, and support processes that require statistical input.
Communicate and collaborate with other project statisticians within R.
Manager, Statistics in Hampshire employer: Pfizer
At Pfizer, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that prioritises employee well-being and professional growth. Our hybrid work model fosters flexibility, allowing you to balance your personal and professional life while contributing to groundbreaking advancements in healthcare. With a commitment to diversity and a focus on empowering our employees, you'll find meaningful opportunities to make a real impact in the lives of patients around the world.
