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Full-time Senior Director role leading discovery and clinical-stage portfolio research project teams in oncology. Responsible for developing innovative scientific project strategies to address unmet medical needs in cancer. Collaborate with stakeholders, lead high-performing teams, manage risks, and contribute to regulatory strategies.
Warehouse Associate III responsible for managing the movement of materials and finished goods within the plant or warehouse. Responsibilities include receiving, storage, inventory control, internal distribution, and shipping in compliance with corporate standards. Must have 4+ years of experience, high school diploma or GED, advanced knowledge of information management practices, and proficiency in operating motorized forklifts and computer software.
The International Tax Manager will be responsible for managing various aspects of private and public Country-by-Country Reporting (CbCR). This role involves data gathering and analysis, XML tagging, regulatory controls, process reengineering, and monitoring the regulatory landscape. The candidate should have recent U.S. international corporate income tax experience and be highly skilled in Excel and XML.
The International Tax Manager will be responsible for managing various aspects of private and public Country-by-Country Reporting and ensuring compliant, accurate, and timely filings. This role involves data gathering and analysis, XML tagging, regulatory controls, process reengineering, and monitoring regulatory activities. The manager will collaborate with various internal departments and external auditors to streamline the reporting processes and improve quality.
As a Senior Manager of Quality Operations at Pfizer, you will be responsible for setting objectives for multiple projects, managing operational activities, ensuring compliance with regulatory filings, and guiding the team towards quality excellence. Your role will involve evaluating clinical and commercial batches of drugs, overseeing audits and inspections, and implementing global quality and compliance expectations.
The Head, Oncology Quality is responsible for providing leadership and oversight of a team of Global R&D Quality Assurance Professionals in support of multiple early and late phase development programs. They ensure compliance and quality assurance activities in clinical trials and development laboratory activities. This role involves coaching staff, interacting with regulatory authorities, and leading global drug development activities.
The Senior Oncology Account Specialist (SOAS) at Pfizer is responsible for promoting Pfizer's product portfolio to healthcare providers, educating the healthcare community on product use, and enhancing patient care quality. The role involves building relationships with key customers and increasing Pfizer's brand presence in the market.
Manage obesity clinical studies at Pfizer, overseeing project timelines, budgets, and objectives. Lead complex projects, resolve issues, manage study operations, budget forecasting, and ensure compliance with regulations. Collaborate with internal and external stakeholders to improve operational efficiencies and deliver successful outcomes.
Manage obesity clinical studies, oversee project management, ensure studies are within time and budget, lead complex projects, resolve issues, manage operational study management, forecast and manage clinical trial budget, provide input to country outreach surveys, oversee drug supply management, evaluate study progress, maintain communications with investigator sites.
As the Director of Study Management for Obesity Programs at Pfizer, you will be responsible for overseeing and directing clinical studies to ensure they are completed within time, budget, and scope. Your role involves setting objectives, managing projects, leading study teams, and making strategic decisions to meet business needs. You will also establish operational standards, promote innovation, and drive the division towards long-term goals.
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