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The Director of Study Management for Obesity Programs at Pfizer will oversee the planning and execution of clinical studies, ensuring they are completed on time and within budget. This role requires collaboration across various functions to drive study timelines and quality targets while also fostering a culture of innovation within the team.
Senior Process Engineer responsible for developing and modifying process formulations, methods, and controls to meet quality standards. Leading product manufacturing campaigns, providing technical supervision, and ensuring compliance with quality and safety standards. Collaborating with stakeholders to assess and transfer processes for new product introduction projects.
As an IPC Coordinator, you will monitor equipment functioning, ensure compliance with SOPs and cGMPs, and assist in training others. You will streamline processes and improve operations while managing your workflow effectively and collaborating with leadership to address training gaps.
The role involves leading the development of novel payloads and linkers for antibody-drug conjugates (ADCs) using computational chemistry techniques. The candidate will analyze drug targets, design ADC components, and collaborate within multidisciplinary teams to enhance drug discovery processes, utilizing both traditional and AI-driven methodologies.
The Senior Scientist will design and execute preclinical research activities focusing on ADCs, collaborating with cross-functional teams. Responsibilities include conducting experiments, analyzing results, and guiding research strategies to advance oncology therapies. The role requires expertise in cancer biology and effective communication skills.
The role supports the Marketing team by providing administrative and operational duties, including producing documents, maintaining presentations, liaising with stakeholders, assisting with projects, and preparing marketing materials.
The Senior Statistical Data Scientist is responsible for ensuring quality datasets and displays for clinical study reports. They will provide documentation and quality control, collaborate with statisticians, and maintain knowledge of safety standards. This role also involves contributing to departmental initiatives and may address complex problem-solving tasks.
The Senior Scientist will lead pre-clinical drug discovery studies for ADC therapies, focusing on in vivo pharmacology studies to assess efficacy, safety, and PK/PD relationships. Responsibilities include designing and executing studies, developing new mouse models, collaborating with cross-functional teams, and managing study timelines, all while ensuring compliance with regulatory standards.
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.
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