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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 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 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 Risk Management & Compliance (RM&C) Lead at Pfizer will oversee compliance quality monitoring, develop remediation plans, and drive risk management priorities across operations. Responsibilities include partnering with leadership for risk awareness, conducting risk analysis, guiding process standardization, and supporting internal and external audits.
The Finance Associate in R&D Oncology will provide financial operations support, including analysis of profit and loss statements, budgeting, forecasting, and financial reporting. They will collaborate with various Oncology teams and Finance Managers to prepare financial information and conduct detailed analyses to guide operational decisions, ensuring accuracy and compliance in financial processes.
The Finance Associate in R&D Oncology will provide financial analysis, budgeting, and forecasting support for Oncology operating lines and Medical Affairs projects. Responsibilities include preparing financial reports, coordinating budgeting processes, and analyzing financial data to assist in decision-making for management and business partners.
The Finance Associate, R&D Oncology will support budgeting, forecasting, and financial analysis for the Oncology R&D organization. Responsibilities include providing financial support for operations, collating data for reports, advising Finance Managers, and ensuring compliance with financial responsibilities. The role involves close collaboration with various internal teams to enhance decision-making through detailed analysis and reporting of financial information.
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