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As a Salesforce Manager at Pfizer, you will lead the administration and support of Salesforce applications, ensure quality and stability of the platform, develop and maintain Salesforce configurations, and manage incident responses. You will collaborate with teams to improve processes, maintain security standards, and support various integration requirements.
The Clinical Study Team Lead at Pfizer is responsible for leading multiple complex global clinical trials, managing timelines, budgets, and quality objectives. They will collaborate with functional leadership to ensure resourcing, drive proactive project planning, and maintain inspection readiness. Strong leadership and effective team performance are key to achieving project milestones and positive patient outcomes.
As a Clinical Study Team Lead, you will manage complex global studies in alignment with therapeutic area strategies, leading cross-functional teams to achieve study timelines, budgets, and quality targets while ensuring optimal resource allocation and risk management.
The Clinical Study Team Lead manages and leads clinical study teams to ensure timely and budget-compliant execution of complex global studies. Responsibilities include strategic planning, risk management, and cross-functional collaboration to meet project deliverables and maintain compliance throughout clinical trials.
As a pharmacometrician, you will conduct quantitative analyses to inform drug safety and efficacy during clinical development, collaborate with multidisciplinary teams, prepare regulatory documents, and contribute to MIDD strategies. You will also mentor less experienced colleagues and participate in improving methodologies used in pharmacometrics.
As a Pharmacometrician, you will perform quantitative analyses related to drug development, collaborate with multidisciplinary teams, and contribute to the planning and execution of modeling strategies. You will prepare presentations, author regulatory documents, stay updated on industry guidelines, and mentor junior staff in pharmacometric knowledge and techniques.
The Senior Director of Clinical Research will lead the development and implementation of clinical studies for novel therapies in respiratory diseases, coordinate with project teams and external investigators, develop and refine trial designs, and ensure safety and quality of studies throughout their lifecycle while fostering collaboration with various research teams.
The Senior Associate in Early Phase Regulatory Affairs will represent the EU region for oncology projects, implementing regulatory strategies, ensuring timely submissions, and maintaining compliance with health authorities. They will collaborate with project teams and manage communications with regulatory agencies to influence the regulatory environment and support project goals.
The Director of Study Management will oversee clinical studies in the Pfizer Biopharma Group, managing timelines, budgets, and resources to ensure compliance with strategic objectives. This role involves leading study teams, coordinating project deliverables, and establishing operational standards to enhance performance and drive innovation in patient care.
The MBA Strategy & Consulting Summer Associate role at Pfizer involves contributing to business strategy development, managing project workstreams, and assessing market trends to inform strategic direction. The associate will work closely with various business units to align strategic priorities and engage in learning opportunities through project participation.
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