Top Tech Jobs & Startup Jobs in NYC, NY

Lead scientific strategy for seasonal viral vaccine program, manage research teams, collaborate with external partners, and oversee project risks and documentation.

The Senior Manager oversees Patient Services vendor programs, ensuring quality governance and operational compliance, while fostering vendor relationships and enhancing program efficiency through data management and continuous improvement practices.

The Director, Strategy & Operations Lead will drive strategic and operational efforts in brand advertising, creative standards, and marketing technology, ensuring organizational goals are met efficiently while fostering a culture of collaboration and innovation.

The Administrative Assistant provides high-level support to the Head of PBAP, managing the calendar, travel, expenses, and facilitates team meetings and operations with a proactive approach.

The role involves leading the Security and Compliance function, ensuring regulatory compliance, fostering business partnerships, and overseeing cybersecurity risk management within a pharmaceutical context.

The role leads medical evidence strategy for adult RSV vaccines, focusing on study design, regulatory interactions, and collaboration with experts in the field. Responsibilities include overseeing research and ensuring compliance with epidemiological methods and strategies while also dealing with data analysis and publication efforts.

The Senior Manager will develop and execute the patient services strategy for Pfizer's Oncology/Specialty Care/Primary Care BU, ensuring alignment with business needs and managing patient service programs effectively.

The Senior Manager of Medical Affairs for Sickle Cell Disease in the US leads strategy development, collaboration with cross-functional teams, and supports medical communication initiatives while mentoring junior staff.

Lead the medical evidence strategy for adult RSV vaccine programs, overseeing studies, regulatory interactions, and collaborations, while ensuring consistency and methodological rigor across projects.

Provide scientific oversight and data quality for late-stage oncology clinical trials; author protocols and regulatory documents; analyze emerging safety and efficacy data; partner cross-functionally to execute phase 3/pivotal programs and support regulatory submissions and governance.