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As a Principal Scientist, you will develop analytical strategies for pharmaceutical products, oversee method validation and stability studies, and lead project activities while collaborating with multidisciplinary teams. You will also author regulatory submissions and mentor peers in a commitment to high-quality standards.
As a Senior Principal Scientist, you will develop and implement cutting-edge analytical processes for biotherapeutics and vaccine products, ensuring they meet regulatory standards. You will contribute to multi-disciplinary teams, lead analytical strategy development, manage project timelines, and mentor junior scientists while ensuring quality and compliance throughout the drug development process.
The Clinical Data Scientist, Manager is responsible for overseeing clinical data operations, ensuring data accuracy and compliance, leading project teams, and collaborating with stakeholders. This role requires strong planning, data management skills, and the ability to guide operational teams in various projects to improve processes and facilitate data integrity.
The Obesity Development Lead will oversee obesity-related clinical programs, manage cross-functional teams, and drive strategy for obesity asset development. This role requires leadership in innovative approaches to maximize asset value and manage business development assessments globally, ensuring alignment with strategic goals.
The Issue Lead is responsible for Quality Event case management, including assessing submitted cases, conducting root cause and gap analyses, escalating critical issues, and developing CAPA plans. The role involves ensuring compliance with timelines and leveraging data for process efficiency and improvement.
The Senior Manager of CRD Operations and External Development will guide the portfolio and operational deliverables within Chemical Research and Development by enhancing partnerships with external development organizations. This includes overseeing laboratory activities, ensuring regulatory compliance and safety, managing resource allocation, and driving programs through the API Development Workflow.
The Senior Associate Scientist, Automation will design and develop laboratory automation solutions, integrating robotic systems and digital tools, while collaborating with a multi-disciplinary team to enhance workflows in pharmaceutical drug development.
The Associate Research Fellow will serve as a subject matter expert in spray dried dispersion technology, collaborating with formulation scientists for drug candidate selection and SDD composition development. Key responsibilities include the evaluation of physicochemical properties, design of SDD formulations, conducting research, and providing laboratory supervision. The role also involves developing predictive models and collaborating with academic and industrial researchers.
The Associate Director of Biostatistics will design, analyze, and interpret clinical trials and observational studies while ensuring compliance with regulatory requirements and Pfizer standards. They will provide statistical expertise in study design, analyses, and communicating results, working collaboratively with cross-functional teams for various clinical development projects and regulatory submissions.
As a Senior Associate Lab Automation Scientist, you will enhance laboratory efficiency by developing and implementing automation, robotics, and data analysis tools. Collaboration with diverse scientific teams is crucial to optimize workflows, integrate systems, and mentor peers. You will improve data access and operational processes using advanced analytical and digital technologies.
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