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As a Senior Associate Scientist, you will support the development and optimization of glycoconjugate vaccines, conduct in-process analysis, collaborate with teams, and ensure compliance with documentation and regulations. You will also participate in technology transfer and provide technical support to the clinical manufacturing site.
The Sr. Development Engineer II will ensure medical devices and drug/device combinations meet intended functions through engineering studies and compliance with corporate procedures. Responsibilities include developing test methods, conducting data analysis, writing reports, and potentially leading project teams. A strong emphasis on teamwork, problem-solving, and technical writing is essential.
The Senior Manager, Solution Engineer at Pfizer will lead the design and development of digital solutions, focusing on creating scalable data pipelines, implementing data quality checks, optimizing data processes, and collaborating with stakeholders across various functions. The role also includes mentoring junior engineers and staying updated with innovative technologies.
The Manager, Data Engineer will lead the development and execution of data infrastructure and pipelines, ensuring data quality and compliance. Responsibilities include collaborating with stakeholders, implementing data monitoring, optimizing data storage, and maintaining documentation. The role involves working with various data platforms and technologies.
The Associate Scientist in Sample Management will receive samples from clinical trials, track and document the chain of custody, manage sample storage and distribution, and comply with regulatory requirements. Responsibilities include using an electronic database, assisting with robotic instruments, and maintaining compliance with SOPs and other guidelines.
The Late-Stage Clinical Scientist oversees clinical trials in oncology, ensuring scientific oversight and data integrity. Responsibilities include supporting trial implementation, authoring regulatory documents, analyzing clinical data, and improving clinical procedures in collaboration with various teams.
The Late-Stage Clinical Scientist manages scientific oversight, data integrity, and quality of clinical trials in oncology. They support clinical teams in protocol authorship, data analysis, and adherence to regulations. Working closely with medical colleagues, they analyze safety profiles and participate in improving clinical procedures within a diverse team.
The Non-clinical Senior Associate Statistician/Data Scientist role involves designing studies, analyzing data, and interpreting results to support drug development. Responsibilities include developing statistical solutions, collaborating across disciplines, and enhancing statistical methods in Pfizer's projects.
The Late Stage Clinical Scientist is responsible for overseeing scientific integrity and quality of clinical trials in oncology, supporting the clinical research team, authoring related documents, reviewing safety data, and ensuring compliance with regulations. The role requires a strong understanding of clinical procedures and effective communication skills.
The role involves managing corporate communications and PR initiatives to enhance Pfizer's reputation in Brazil. Responsibilities include defining communications strategies, managing media relations, participating in industry associations, coordinating special events, and supporting internal communication efforts. The position also requires crisis management and media training.
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