Pfizer

This role focuses on epidemiological research within healthcare, specifically for drug safety surveillance. It involves conducting literature reviews, designing database studies to assess risks and effectiveness of interventions, and engaging with regulatory agencies. While the role mentions using AI tools like ChatGPT, AI/ML is not the core craft.

Pfizer is seeking a Clinical Development Medical Director to serve as a clinician within a vaccine development program. This role involves providing medical and scientific expertise and oversight for clinical trials, ensuring patient safety, contributing to protocol design and strategy, supporting study teams, and interacting with regulatory authorities and key opinion leaders. The position requires accountability for the medical and scientific validity of study reports and disclosures.

Pfizer is seeking a Director of Vaccines Clinical Research (MD required) to provide medical and scientific expertise for clinical trials, ensuring patient safety and overseeing study design, execution, monitoring, delivery, and reporting. The role involves designing development strategies, participating in committees, reviewing compounds for in-licensing, and supporting new business development. Responsibilities include managing safety surveillance, protocol design, study team support, data interpretation, regulatory document authorship, and interactions with regulatory authorities, key opinion leaders, and principal investigators.

Pfizer is seeking an Oncology Field Medical Director with expertise in Malignant Hematology to provide therapeutic area and product knowledge to healthcare professionals in an assigned territory. The role involves executing medical strategy, serving as a conduit for medical information and customer insights, supporting clinical trial identification and the Investigator Sponsored Research process, and collaborating with internal and external stakeholders.

Clinical Research Manager for Oncology in Japan, responsible for clinical development strategy, execution, and regulatory submissions under the supervision of the Japan Development Leader. Collaborates with global teams, KOLs, and internal stakeholders to advance drug projects.

This role at Pfizer focuses on clinical research and development within the healthcare domain. The Sr. Clinician will co-chair clinical study teams, provide clinical and scientific expertise for protocol development, and ensure efficient clinical trial design. Responsibilities include writing protocols, managing study risks, overseeing data quality, selecting sites and investigators, and ensuring regulatory compliance. The role also involves site liaison activities to support trial conduct and maintain relationships with site staff. It requires a deep understanding of disease areas and indications, and may involve mentoring less experienced clinicians.

Responsible for the clinical development of assigned projects in Japan, working under the supervision of the Japan Development Leader. This role involves formulating and executing global and Japan development strategies, evaluating candidates, leading clinical studies, and preparing documentation. Requires strong scientific, leadership, and project management skills, with fluency in both Japanese and English.

Statistician role at Pfizer focused on clinical trial design, analysis, and interpretation, ensuring compliance with regulatory requirements and company standards. The role involves collaborating with clinical development teams, providing statistical expertise, and contributing to drug development plans and regulatory submissions. Requires advanced statistical skills, understanding of drug development, and knowledge of clinical medicine and regulations.

Responsible for statistical operations related to clinical trials and regulatory submission documents for vaccine projects. This includes creating and managing the quality of statistical analysis plans, providing statistical advice on development plans and protocols, and supporting programming tasks as needed. The role involves global collaboration and reporting directly to Global Vaccine Research.

Seeking a Principal Scientist for Downstream Process Development in Bioprocess R&D. The role involves hands-on laboratory research to develop and optimize recovery and purification processes for recombinant proteins, supporting clinical programs. Responsibilities include designing studies, analyzing data, contributing to process characterization and validation, authoring reports, and providing technical leadership.

Associate Director, Research and Development for Vaccines at Pfizer in Japan. This role involves providing medical and scientific expertise for clinical trials, contributing to protocol design and development strategy, ensuring patient safety across studies, and interacting with regulatory authorities and key opinion leaders. The position requires a medical degree and licensing, with a focus on the Japan and Asia-Pacific regions.

This role is for a Medical Affairs Scientist at Pfizer, focusing on building relationships with healthcare professionals and stakeholders to advance patient outcomes. The scientist will generate and share medical insights, manage external engagements, and collaborate with internal teams. The role requires an advanced scientific degree and pharmaceutical experience, with a strong emphasis on stakeholder management and compliance within the healthcare and pharmaceutical industry.

This role focuses on developing synthetic routes and scalable chemical processes for novel small molecule components in targeted therapeutics within the pharmaceutical industry. It involves route scouting, process development, and characterization, applying principles of organic chemistry and process research. The role also includes mentoring junior scientists, leading cross-functional teams, and overseeing GMP production batches.

This role is for a Development Head overseeing vaccine clinical research and development programs at Pfizer. The position requires extensive expertise in clinical research, program design, and regulatory activities to ensure successful implementation and registration of vaccine candidates. Responsibilities include leading global clinical research programs, providing scientific and procedural expertise, managing clinical project teams, and ensuring quality and safety across studies. The role also involves potential in-licensing reviews and contributing to business development. A medical degree and over 10 years of pharmaceutical industry experience in clinical research are required, with specific experience in end-to-end vaccine clinical development.

Clinical Development Scientist, Director role at Pfizer focused on providing medical and scientific leadership for clinical trials in Inflammation and Immunology. Responsibilities include protocol development, study execution, data interpretation, risk management, and contributing to regulatory filings. Requires a PhD/PharmD with 5+ years of experience or MS with 7+ years, or BS/BA with 8+ years in a relevant science discipline, with deep knowledge of clinical development, ICH/GCP, and global regulatory requirements.

Pfizer is seeking a Global Development Lead (MD, Sr. Director) for Internal Medicine to lead clinical development for assigned assets. This role involves designing, executing, and interpreting clinical studies, creating clinical development plans, and partnering with cross-functional teams and external stakeholders. The position requires extensive knowledge of clinical development, global regulations, and experience managing large teams in the biopharmaceutical industry.

This role is for a Senior Associate Scientist in Pharmaceutical Research and Development at Pfizer, focusing on the formulation development and analytical characterization of biotherapeutics. The scientist will use various biophysical and biochemical techniques, support drug product manufacturing process development, and be responsible for data compilation and reporting. The position requires a Bachelor's or Master's degree in a relevant scientific field with 0-4 years of experience.

Seeking a Principal Scientist with expertise in enzymatic peptide synthesis and biocatalysis for innovative process development in peptide and API manufacturing. Requires a PhD and strong experimental skills, with industry experience preferred. Role involves designing, optimizing, and scaling enzymatic processes, collaborating cross-functionally, and contributing to scientific innovation.

Seeking a VP, Global Head of Statistics for Vaccine Clinical Research and Development (VCRD) to set vision and provide leadership for data management, modeling, and statistical advice across a complex portfolio of clinical development projects. This role requires deep expertise in statistical analysis tools, regulatory guidelines (FDA, ICH), and managing a large team of statisticians and modelers.

Pfizer is seeking a Clinical and Translational Biomarker Lead to develop and implement biomarker strategies for assigned assets in weight management and cardiometabolic disease. This role involves scientific and technical leadership, managing external and internal partners for biomarker assays and data, and contributing to clinical development plans, regulatory filings, and publications. The lead will oversee assay lifecycle management, manage external laboratories, and interpret biomarker results in the context of clinical studies.

Pfizer is seeking a Director-level Clinical Development Scientist for their Oncology portfolio. This role involves scientific oversight, data integrity, and quality of clinical trials, partnering with cross-functional teams, authoring study documents, and analyzing emerging safety and clinical data. Requires extensive experience in clinical research, particularly in Phase 3 Oncology trials, and a strong understanding of regulatory guidelines.

This role is for a Senior Manager in Oncology Clinical Development at Pfizer, responsible for scientific oversight, data integrity, and quality of clinical trials. The position involves authoring protocols, reviewing clinical data, analyzing safety profiles, and ensuring compliance with regulations and SOPs. It requires a strong background in clinical research within the oncology space, experience with large datasets, and collaboration with cross-functional teams.

Clinical Development Medical Director (Associate Director) at Pfizer responsible for medical and scientific oversight, data integrity, and quality of clinical trials in Internal Medicine. This role involves providing medical monitoring, clinical support, protocol design input, and contributing to regulatory filings and reporting.

This role supports the development of parenteral formulations for antibody–drug conjugates (ADCs) and monoclonal antibodies (mAbs) within Pfizer's biotherapeutics portfolio. Responsibilities include formulation development, analytical characterization using biophysical and biochemical techniques, supporting drug product manufacturing process development, and technical report writing. The role requires a Bachelor's or Master's degree in a relevant scientific discipline and hands-on laboratory experience with analytical techniques.

This role supports the development of parenteral formulations for antibody-drug conjugates (ADCs) and monoclonal antibodies (mAbs) within Pfizer's biotherapeutics portfolio. Responsibilities include performing formulation development, analytical characterization using various biophysical and biochemical techniques, supporting drug product manufacturing process development, and data compilation/reporting. The role requires a Bachelor's or Master's degree in a relevant scientific field and hands-on laboratory experience with analytical techniques.

Medical Director for Oncology Clinical Development at Pfizer, providing leadership for clinical trials, ensuring scientific, ethical, and regulatory standards are met, and collaborating with various functions and external stakeholders.

This role focuses on clinical pharmacology and Model-Informed Drug Discovery and Development (MIDD) within Pfizer's Internal Medicine portfolio. The lead will provide expertise in pharmacokinetics, pharmacodynamics, and patient characteristics to inform drug development strategies, study designs, and regulatory interactions. Responsibilities include designing and executing clinical pharmacology plans, overseeing study activities, and contributing to regulatory documents. Strong quantitative skills in PK/PD modeling and clinical trial simulations are required.

This role focuses on early drug discovery, specifically hit identification and lead optimization for small molecule drug discovery. The Principal Scientist will design and execute in vitro assays, investigate mechanistic pharmacology, and collaborate with cross-disciplinary teams. The role requires expertise in biochemistry, cell biology, and pharmacology, with a strong emphasis on assay development and troubleshooting.