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Join a team of scientists supporting oncology development programs as the Clinical Pharmacology Lead. Provide clinical pharmacology expertise to project teams, contribute to regulatory documents, and support PK/PD analyses.
Monitor drug, biologics, and medical devices surveillance program, intake and processing of adverse reports, support clinical trial and post marketing activities
Review, prepare, and complete clinical study adverse event reports to determine the safety profile of Pfizer's products and meet regulatory requirements. Conduct data entry, case assessment, processing, and documentation. Liaise with key partners and participate in safety activities. Bachelor's degree in a science-related field required.
As the Senior Director, Statistics Lead at Pfizer, you will provide scientific leadership and technical support for clinical and non-clinical projects. Responsibilities include developing innovative statistical solutions, leading projects, providing statistical advice, and promoting statistical methodologies. You will collaborate with various stakeholders and external partners to advance drug development methodologies.
Oversee vaccine clinical research and development programs, lead global clinical research programs, provide strategic solutions to program issues, collaborate with clinical teams, and ensure quality and timely completion of clinical trials and documents.
Oversee and ensure vaccine clinical research and development program implementation to meet company objectives. Lead global clinical research programs and registration activities. Identify and advance innovative strategies to solve clinical issues. Provide procedural and scientific expertise to guide global trial leaders and clinical staff. Design development strategies for worldwide approval of compounds or vaccines.
The Vice President of Vaccine Clinical Research & Development will oversee and ensure that vaccine clinical research and development programs are planned and implemented to meet company objectives. Responsibilities include leading global clinical research programs, providing high-level oversight, identifying program issues, collaborating with clinical leads, and assuring program quality through oversight and monitoring.
Oversee and ensure vaccine clinical research and development program(s) are planned and implemented to meet company objectives. Lead global clinical research programs and registration activities. Provide high-level oversight of program direction, prioritize key programs, collaborate with clinical leads, and assure quality through the clinical trial cycle. Administer and oversee clinical lead and clinician activities.
Oversee companion diagnostic strategy for clinical oncology development programs, provide regulatory expertise, collaborate with cross-functional teams, and lead diagnostic testing strategies from early to late-stage programs.
The Senior Manager of Clinical Diagnostics will oversee companion diagnostic strategy for multiple late and early-stage clinical oncology development programs. Responsibilities include designing strategic recommendations, providing oversight, and collaborating with various functions to drive diagnostic and clinical testing strategy from IND to Launch.
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