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The Principal Scientist will lead in vivo pharmacology efforts for drug discovery projects, focusing on ADC Biology and Cancer Immunology. Responsibilities include collaborating with teams, supervising staff, designing and conducting in vivo studies, ensuring regulatory compliance, and presenting findings in reports and publications.
Senior Associate, Principal Statistical Data Scientist responsible for statistical programming deliverables in the pharmaceutical industry. Mentor junior team members, handle complex programming tasks, adhere to high-quality standards, and collaborate with global stakeholders. Bachelor's or Master's degree in relevant field with 5-6 years of experience required.
Hands-on programming role supporting statistical programming deliverables, collaborating with senior programmers, adhering to programming standards, ensuring timely completion of tasks, collaborating with study teams and stakeholders, self-learning and delivering solutions in statistical programming and data standards, contributing to global and local initiatives
As a Tele-Marketing Protégé, you will gain essential skills and hands-on experience in tele-marketing through comprehensive training and mentorship. Responsibilities include making outbound calls, understanding products, and maintaining customer interaction records.
The Senior Principal Scientist will lead in vivo pharmacology efforts in drug discovery projects, supervise laboratory staff, ensure compliance with regulations, develop new mouse models for cancer research, and contribute to study reports and publications.
The Principal Statistical Data Scientist will oversee multiple projects, ensuring deliverables meet CDISC aligned standards. They will validate datasets, execute code runs, support project requirements, and mentor junior team members while collaborating with global stakeholders on project goals.
The QA Coordinator is responsible for managing change control and document control systems at the KAEC site, ensuring compliance with GMP regulations and Pfizer standards. This includes overseeing training programs, coordinating documentation, and preparing reports related to training and process management.
The Oncology Field Medical, Director is responsible for executing medical strategies and engagements, providing therapeutic expertise, optimizing communication, and supporting medical content delivery. This role involves collaboration with medical colleagues, responding to HCP requests, and engaging in patient advocacy and research initiatives.
The Oncology Field Medical Director is responsible for medical strategy and engagement within the therapeutic area. This role involves communicating product knowledge to stakeholders, leading advisory boards, collaborating with medical teams, and supporting clinical trial site identification. The director ensures patient-centered communication and provides accurate medical information to healthcare professionals while maintaining compliance with Pfizer guidelines.
The Oncology Field Medical Director manages medical strategy and engagement within their designated territory, providing expertise on therapeutic areas and Pfizer products. Responsibilities include delivering medical information to healthcare professionals, collaborating with colleagues, and optimizing patient-centric communications while leading efforts in clinical trials and research initiatives.
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