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Posted Today
The incumbent is responsible for supporting VRD vaccine programs, has primary scientific responsibility in the evaluation of vaccine candidates. The incumbent is expected to develop, qualify, and transfer diagnostic and serologic immunoassays in support of Vaccine Programs. He\she is expected to propose, plan, and implement experimentations in a cohesive manner that addresses assigned research obj
Posted Today
The role of the incumbent is to assist in the lab based development and qualification of molecular biology assays for testing vaccine products. The incumbent will also be involved in the high throughput clinical testing of human nasopharyngeal swabs and blood samples. This role will be responsible for RNA and DNA extraction, real time PCR, handling bacterial and/or viral stocks and human pre clini
Posted Today
The candidate will perform and supervise lab based development and validation of molecular biology assays for testing clinical samples in a regulated environment. Incumbent will also handle multiple aspects of day to day laboratory management including task assignment for junior lab staff members, project coordination and data presentation. Must be experienced in PCR, molecular biology techniques
Posted Today
The incumbent contributes to programs that apply molecular biology toward expressing vaccine antigens of interest in bacterial culture. Support of a program that seeks to optimize in vitro transcription and template preparation is in scope. The position is also responsible for preparing plasmids for expression of recombinant proteins, primarily in E coli. Responsibilities also include systematic c
Posted Today
The role of the incumbent is to assist in the lab based development and qualification of ligand binding immunoassays for the detection of antibodies to novel candidate vaccines in support of candidate vaccine programs. The incumbent will also be involved in testing of pre clinical and clinical sera samples. Responsibilities include generation and characterization of reagents, performance of experi
Posted Today
The Field Medical Director (FMD) is a field based medical colleague responsible for providing therapeutic area /product expertise for the designated therapeutic area in the assigned region (comprised of one or more US states) focusing on the therapeutic area's in line and late stage portfolio. The responsibilities of the FMD are to contribute to Pfizer's ability to (a) communicate new and other im
Posted Today
The Field Medical Director (FMD) is a field based medical colleague responsible for providing therapeutic area /product expertise for the designated therapeutic area in the assigned region (comprised of one or more US states) focusing on the therapeutic area's in line and late stage portfolio. The responsibilities of the FMD are to contribute to Pfizer's ability to (a) communicate new and other im
Posted Today
Pfizer
- St. Louis, MO / Lake Forest, IL / New York, NY
Pfizer Digital is a customer oriented, front line organization with a vision to Win the Digital Race in Pharma and Unleash the Power of our Colleagues by creating compelling digital HR experiences for our internal and external audiences. As a team member, and in partnership with Pfizer's HR organizations, the selected candidate will manage end to end delivery of HR technology solutions and ongoing
Posted Today
Pfizer
- Collegeville, PA / Groton, CT / La Jolla, CA / 1 more...
The purpose of the position is to lead regulatory affairs capability for a specific therapeutic category within Global Product Development. The incumbent would typically have the single point accountability for the Oncology Triad. The incumbent serves as a senior regulatory leader who has global mindset and expertise of drug development and product lifecycle processes and priorities, regulatory en
Posted Today
Pfizer
- Pearl River, NY / New York, NY / Rouses Point, NY
This position can be based remotely anywhere in the United States The Study Start Up Project Manager is responsible for defining, developing and delivery of the Global Study Start Up Project Plan by partnering with Study Manager, Clinical Trial Application Group, Site Activation Partners, CRO Study Start Up and Site Relationship Partners and others as required for Phase 3 and other supported studi
Posted Today
Pfizer
- Bridgewater, NJ / New York, NY
The Vendor Quality Lead (VQL) reports to the Head of Sourcing Oversight & Contracting Compliance. The VQL is responsible for driving the Vendor Quality Risk Framework and Vendor Quality Plans for Central Lab, Sample Management, ECG and eCOA vendors,. The VQL serves as the point person to stakeholders and relevant oversight teams for vendor quality risk management, vendor quality issues management
Posted Today
Pfizer
- Pearl River, NY / Collegeville, PA
This position will provide statistical support for clinical Phase I IV projects in Vaccine Research and Development. The successful candidate will collaborate with study teams working effectively to design studies, develop protocols, write statistical analysis plans, perform statistical analysis, write reports, present results summarizing findings, develop publications of results, contribute to ov
Posted Today
The Manager, Health Economics & Outcomes Research (HEOR) Eliquis is responsible for execution of high quality HEOR strategic efforts to support optimal reimbursement and access for Eliquis globally, with a focus on delivering robust evidence demonstrating the clinical and economic value of the product(s), successfully impacting business objectives on a global basis. As part of the Global HEOR
Posted Today
Global Procurement delivers world class procurement capabilities to Pfizer, partnering with internal Pfizer customers to ensure they receive maximum value for every dollar spent with Pfizer suppliers. We accomplish this by executing effective strategic processes, including category management, supplier management and sourcing projects, all supported by efficient procure to pay processes. We add va
Posted Today
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