The Viral Vaccine group is seeking a non PhD scientist to join our highly dynamic team in vaccine research and development. The incumbent is responsible for supporting the antigen discovery, antigen optimization, and the assessment of protein quality. The incumbent will assist with protein expression in bacterial and mammalian suspension cell culture and protein purification using various chromato

Asset Program Development, Strategy, and Planning Working with Asset Team leadership, leads development of integrated program plans (e.g., Development, Lifecycle, and Operating plans) and ensures alignment with the overall candidate strategic plan and operational and Partner Line plans for the program scope, which may span from Lead Development to Loss of Exclusivity. Drives decision point plannin

The Submission Medical Writer creates documents pertaining to clinical data and post marketing safety data to support product development, license application, and post marketing maintenance on behalf of and in conjunction with corresponding project teams. Some examples of such documents include briefing documents to support meetings with regulatory agencies, clinical documents for marketing autho

This position will be responsible for developing and execution of Pfizer's vision and strategy in hematology/multiple myeloma and will lead agents and the clinical development team associated with the agent (s) within Oncology Clinical Development. Leader will provide strategic and technical guidance at an agent and or indication level within Oncology Clinical Development, as well as enterprise wi

Last Date to Apply for Job October 14, 2020 Eligible for Employee Referral Bonus YES #LI PFE Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, addre

We have an exciting opening for a Clinical Pharmacology Lead. Pfizer is a leader in model based drug development and you will be an integral member of the Pfizer Clinical Pharmacology team, supporting late stage programs in the Internal Medicine therapy area. The colleague will initially work under the guidance of an experienced Clinical Pharmacology Lead to provide required clinical pharmacology

Provide pharmacometric expertise and leadership to projects in support of the oncology portfolio. Develop model informed drug development (MIDD) plans in support of projects and more broadly across disease areas in oncology in order to optimize prospective studies, inform drug development strategy and project decision making, in collaboration with partners. Plan, conduct and report quantitative an

Coordinates implementation of the global biosafety program. Provides technical capability to evaluate the biosafety risk profile (associated with internal operations and external sourcing) and works with direct team and site biosafety organization to develop risk management programs. Contributes to R&D EHS program development (with focus on laboratory and biological safety) to ensure EHS risks

As part of the Data Monitoring and Management group, an integral delivery unit within the Global Product Development (GPD) organization, the Clinical Data Scientist is responsible for timely and high quality data management deliverables supporting the Pfizer portfolio. The Clinical Data Scientist designs, develops, and maintainskey data management deliverables used to collect, review, monitor, and

The Quality Operations Manager assures compliant manufacturing procedures, equipment, and facilities in the new aseptic manufacturing plant in adherence with cGMP requirements, Quality Standards, and other regulatory requirements. This position is part of the project team designing and building the new aseptic facility. ROLE RESPONSIBILITIES Quality SME with GMP input and guidance for the followin

The Quality Operations Manager assures compliant manufacturing procedures, equipment, and facilities in the new aseptic manufacturing plant in adherence with cGMP requirements, Quality Standards, and other regulatory requirements. This position is part of the project team designing and building the new aseptic facility with additional focus on the filling and freeze dry portions of the facility. R

The Senior Manager BSL3 Operations leads the administrative and management support of BSL/ABSL 3 laboratories in the Pearl River. Working alongside Comparative Medicine Program counterpart, the Senior Manager oversees the establishment and implementation of bio safety, security, and common laboratory standard operating procedures and processes in Pfizer Pearl River Bio safety Level 3 laboratories

As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager develops and maintainskey data management deliverables used to collect, review, monitor, an

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; Regu

Last Date to Apply February 15,2020 Eligible for Employee Referral Bonus Eligible for Relocation Package Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's