Pfizer

Seeking a Postdoctoral Fellow to develop AI/ML enabled bioprocess models and control strategies for recombinant protein production. The role involves creating hybrid mechanistic-data driven models, integrating omics data, applying ML/DL for prediction, and exploring agentic AI for model orchestration and transfer learning. Responsibilities include designing experiments, implementing model predictive control, validating models, and communicating results.

Seeking a Postdoctoral Fellow to develop AI/ML enabled bioprocess models and control strategies for recombinant protein production. The role involves creating hybrid mechanistic-data-driven models, integrating omics data, applying ML for prediction, and developing model predictive control frameworks. It also includes exploring agentic AI for orchestrating model fitting and transfer learning, and designing experiments for data generation and validation.

This role focuses on safety surveillance research within the healthcare domain, involving epidemiological studies, literature reviews, and risk assessment for Pfizer products. While the role mentions using AI tools like ChatGPT, it is not the core craft, and the primary focus is on traditional epidemiological research and data analysis.

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.

This role is for a Clinical Leader in Oncology R&D at Pfizer in Japan. The primary responsibilities include leading the clinical development of assigned projects, formulating and executing development strategies in Japan in collaboration with global teams, and managing clinical studies. The role requires a strong scientific background, experience in clinical development and regulatory submissions, and excellent leadership, communication, and project management skills.

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.

Pfizer is seeking a Principal Scientist for their Downstream Process Development group. This role focuses on laboratory research for the development and optimization of recovery and purification processes for recombinant proteins, supporting clinical programs. The candidate will lead small-scale studies, analyze data, contribute to process characterization and validation, author technical reports, and provide scientific leadership.

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 statistical operations related to clinical trials and regulatory submission documents for vaccine projects. This includes creating and quality-controlling statistical analysis plans, providing statistical advice on development plans and protocols, and supporting programming tasks as needed. The role involves global communication and collaboration within the Development Japan team.

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, establishing relationships with stakeholders, leading clinical studies, preparing documentation, and managing clinical data and safety reviews.

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.

Associate Director, Research and Development for Vaccines at Pfizer in Japan. This role involves providing medical and scientific expertise for clinical trials globally, with a focus on Japan and the Asia-Pacific region. Responsibilities include protocol design, ensuring patient safety across studies, supporting study teams, interacting with regulatory authorities and key opinion leaders, and contributing to regulatory documents and publications. Requires a medical degree and prescribing license.

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.

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 assay delivery, 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. The role involves scientific oversight, data integrity, and quality of clinical trials, partnering with cross-functional teams, authoring study documents, and analyzing emerging clinical data and safety profiles. Requires extensive experience in clinical research, oncology, ICH guidelines, GCP, and regulatory affairs.

Pfizer is seeking a Senior Manager for Oncology Clinical Development Scientists. This role involves scientific oversight, data integrity, and quality of clinical trials within the Oncology portfolio. Responsibilities include authoring protocols, setting clinical data review strategy, analyzing safety profiles, and ensuring compliance with regulations. The role requires extensive experience in clinical research, oncology, and understanding of regulatory guidelines.

Pfizer's Health Technology Assessment (HTA), Value & Evidence (HV&E) team is seeking a Director to lead the development and execution of global evidence generation strategies for Obesity treatments. This role focuses on health economics and outcomes research (HEOR) to support patient access and inform healthcare decision-making. The Director will manage HEOR studies, develop launch deliverables, and partner with internal and external stakeholders to ensure optimal patient access.

Principal Scientist role in Analytical Research and Development at Pfizer, focusing on GMP analytical readiness for small molecule drug components. Responsibilities include managing analytical testing, method validation and transfer, evaluating vendor data, and collaborating with project teams. Requires expertise in analytical chemistry and chromatography, with a strong understanding of GMP and drug development workflows.

Scientist with expertise in next generation sequencing (NGS) to support vaccine research and development. Primarily a laboratory-based role involving execution of NGS protocols, sample preparation, library construction, and data analysis. Requires strong molecular biology and analytical skills.

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, contributing to protocol design, data review, safety monitoring, and potentially contributing to regulatory filings. The position requires a primary medical degree and independent prescribing license, with preferred qualifications including cardiometabolic disease experience and a strong track record in pharmaceutical development.

Pfizer is seeking a GU Oncology Field Medical Director to provide therapeutic area and product expertise to healthcare customers in an assigned territory. This role involves executing medical strategy, maintaining knowledge of oncology and Pfizer medicines, serving as a resource for medical information, and collaborating with internal and external stakeholders. The position requires strong communication and interpersonal skills, the ability to manage projects remotely, and significant travel.

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 is an internship role for a medical student or physician in pharmacology at Pfizer in Colombia. The role involves providing medical and scientific support, reviewing promotional materials for compliance, analyzing candidate products, and responding to medical information inquiries. It requires knowledge of the Colombian healthcare system, regulatory procedures, and medical databases.

Associate Scientist role at Pfizer focused on drug metabolism studies using analytical techniques like HPLC/MS and NMR. Responsibilities include sample preparation, metabolite characterization, data analysis, and documentation within a research and development setting.

Associate Scientist role at Pfizer focused on generating immunoassay data for preclinical vaccine programs, performing various assays to monitor immune responses, and contributing to assay improvements. Requires a BA/BS with 0-2 years of lab experience and training in aseptic technique and cell culture.

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 Pfizer's biotherapeutics portfolio by developing parenteral formulations for ADCs and mAbs. Responsibilities include formulation development, analytical characterization using biophysical and biochemical techniques, supporting drug product manufacturing process development, and data compilation/reporting. Requires a Bachelor's or Master's degree in a relevant science field with laboratory experience and strong analytical and communication skills.

Pfizer is seeking a Global Development Lead (GDL) with an MD or DO to lead clinical development for assigned assets in Internal Medicine. The role involves leading cross-functional teams in designing, executing, and interpreting clinical studies, managing regulatory submissions, and contributing to product labels and safety reports. The ideal candidate will have extensive experience in clinical research and development, global regulations, and team management, with a strong track record in pharmaceutical development and medical/scientific credibility.

This role focuses on the formulation development and analytical characterization of biotherapeutic molecules for Pfizer's biotherapeutics portfolio. The Senior Associate Scientist will perform experiments using various biophysical and biochemical techniques, support drug product manufacturing process development, and be responsible for data compilation and reporting. The role requires a Bachelor's or Master's degree in a relevant scientific discipline and hands-on laboratory experience with analytical characterization of biotherapeutics.

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.

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.

Pfizer is seeking a VP, Global Head of Statistics for Vaccine Clinical Research and Development (VCRD) to set the vision and provide leadership for data management, modeling, and statistical advice. This role involves planning and directing complex clinical development projects, interpreting results from various studies, and developing new initiatives. The individual will lead statisticians and modelers, provide senior management review of documents, and act as a senior representative to internal committees. They will influence cross-functional activities and advise on the evolving capabilities and training needs of the VCRD Statistics group, ensuring compliance with regulatory guidelines.

This role provides Clinical Development leadership and expertise on clinical trials within the oncology program, overseeing design, conduct, and analysis. It involves close collaboration with various functions like regulatory affairs, pharmacovigilance, biostatistics, and medical affairs to ensure adherence to scientific, ethical, and regulatory standards. The medical director also offers medical expertise to clinical operations, investigators, and external stakeholders, including health authorities and patient advocacy groups. Responsibilities include study-level clinical development leadership, medical monitoring, peer-to-peer interactions with investigators, and serving as a point of contact for clinical issues. The role also involves contributing to clinical trial and regulatory documents, interpreting clinical data, and staying updated on the latest developments in the field.

Pfizer is seeking a Clinical Development Medical Executive Director to lead and execute the development strategy for oncology programs, specifically in prostate cancer. This role involves leading clinical development teams, designing and overseeing clinical trials, interpreting data, and interacting with regulatory authorities and external stakeholders. The position requires a medical degree or advanced degree with significant clinical and industry experience, including late-phase drug development and team leadership.

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 dosage regimens. Responsibilities include designing and executing clinical pharmacology plans, contributing to regulatory documents, and influencing the external scientific environment through publications and presentations. Requires strong quantitative skills in PK/PD modeling and clinical trial simulations.

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.

Principal Scientist in Pharmacology at Pfizer focused on small molecule drug discovery, hit identification, and lead optimization. The role involves designing and executing in vitro assays, investigating mechanistic pharmacology, and collaborating with cross-disciplinary teams. Requires expertise in biochemistry, cell biology, and pharmacology with a strong knowledge base in scientific advancements.

Clinical Development Scientist, Director role at Pfizer focusing on Inflammation and Immunology portfolio. Responsibilities include providing medical and scientific leadership for clinical trials, ensuring clinical integrity, scientific quality, and patient safety. Key tasks involve protocol development, study execution, data interpretation, risk management, and serving as the primary clinical contact for investigators and internal study teams. The role also contributes to regulatory filings and clinician development through matrix leadership.

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.