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The Late Stage Clinical Scientist is responsible for overseeing quality and integrity in clinical trials within the Oncology portfolio. They author essential clinical documents, analyze safety data, ensure compliance with regulations, and guide cross-functional teams towards successful trial execution. Leadership in mentoring may also be part of their role.
The Late-Stage Clinical Scientist will support the scientific oversight and data integrity of clinical trials in Oncology. Responsibilities include authoring clinical documents, analyzing safety and efficacy data, ensuring compliance with regulations, and leading clinical procedures. The role also involves collaboration with various internal and external stakeholders and may include mentoring others.
The Late-Stage Clinical Scientist will oversee scientific oversight, maintain data integrity and quality in clinical trials, author clinical documents, analyze clinical data, and mentor team members. This role requires collaboration with clinical and medical colleagues to execute trial strategies in oncology and improve clinical development procedures.
The Director, GCS Business Technology Integration will lead the transformation of Pfizer's clinical supply chain systems. This includes implementing technology and digital systems to enhance operations and customer service. Responsibilities involve overseeing the entire lifecycle of supply chain systems, driving process improvements, collaborating with cross-functional teams, managing budgets, and ensuring regulatory compliance while maximizing efficiency and effectiveness.
The Senior Scientist - Process Modeler will develop computational tools and models to support continuous drug manufacturing. Responsibilities include collaborating with project scientists to identify challenges, executing modeling plans, and developing predictive tools using various computational techniques. The role requires communication of results and validation of models through experimental studies.
The Senior Associate will manage and process clinical data, ensuring accuracy and consistency through data management plans. Responsibilities include working with cross-functional teams to create data capture solutions, leading technical initiatives, and serving as a subject matter expert.
As a Global Study Manager II at Pfizer, you'll manage obesity clinical studies, ensuring projects are completed on time and within budget. You will develop plans, resolve complex issues, oversee drug supply management, and work collaboratively with various stakeholders to improve operational efficiencies and achieve study objectives.
As a Senior Manager for obesity clinical studies at Pfizer, you will manage project timelines, budgets, and complex study operations, ensuring compliance and effective communication with all stakeholders involved. You will lead cross-functional teams to achieve operational goals and troubleshoot issues that arise during the study.
As a Director of Biostatistics at Pfizer, you will provide scientific leadership, assist with complex study designs, and collaborate with various teams on clinical and non-clinical projects. Your role will involve the development and implementation of statistical methodologies, ensuring adherence to regulatory guidelines, and fostering collaborations across various domains to advance drug development.
The Director of Biostatistics will provide scientific leadership and technical support for Pfizer's clinical and non-clinical projects, focusing on complex study designs, data analyses, and the development of specialized software. The role emphasizes collaboration across various therapeutic areas, training, methodological research, and external scientific collaborations to enhance statistical methodologies for drug development.
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