Top Operations Jobs
The Senior Manager/Associate Director Medical Writer creates and oversees clinical documents for regulatory interactions, manages document development processes, collaborates with cross-functional teams, and drives project timelines. They ensure compliance with regulatory standards while identifying and communicating potential issues or improvements.
The Senior Manager/Associate Director of Medical Writing creates and manages various clinical study documents and ensures compliance with regulatory requirements. They lead project teams, develop timelines, and communicate with cross-functional teams to produce high-quality documents while identifying areas for process improvement.
The Senior Manager/Associate Director Medical Writer creates and manages clinical documents and regulatory submissions. Responsibilities include independently writing complex documents, managing document development processes, collaborating with teams, maintaining timelines, and ensuring quality. They also drive strategies for data presentation and identify areas for process improvement while serving as the primary contact for document-related issues.
As a Senior Production Operator, you will manage work orders, ensure compliance with safety guidelines, provide technical training, monitor manufacturing processes, maintain documentation, and contribute to process improvements. You will work collaboratively within the Technical Operations team to drive efficiency and quality in drug production.
As a Manager, PI Historian SME, you will oversee manufacturing information systems to enhance success rates and minimize downtime. Key responsibilities include providing constant support for the PI data historian, collaborating with infrastructure leads, coordinating activities, and training personnel while adhering to safety practices.
The Global Transparency Reporting Manager is responsible for ensuring high-quality, accurate data for healthcare transparency disclosures, managing data integrity and compliance with public disclosure laws. This role involves reconciling financial data, collaborating with business leaders, monitoring data quality, and ensuring timely reporting of transparency standards.
The Investigator Contracts Lead manages site-facing contract and budget negotiations for clinical investigator sites. Responsibilities include leading pre-contract activities, negotiating costs, resolving issues during the contracting process, developing relationships with key sites, and ensuring compliance with organizational procedures.
The Field Medical Manager is responsible for stakeholder engagement, executing medical initiatives, and developing external strategies in alignment with the Country Medical Director. The role includes managing field-based medical functions, collaborating on medical projects, and ensuring compliance with internal regulations.
The Regulatory Affairs Department Assistant will provide comprehensive administrative support to the Pfizer Regulatory Affairs Division including document management, system updates, schedule coordination, and project support. Responsibilities encompass organizing meetings, maintaining office materials, and assisting in financial processes.
The ISE India Lead is responsible for delivering strategic analytics and insights to support Pfizer's commercial strategy. This role involves leading cross-functional teams to solve complex business issues, drive performance measurement, engagement with business leaders, and development of analytic solutions. The lead acts as a strategic advisor to senior leadership and ensures team collaboration to meet business objectives.
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