Boehringer Ingelheim is a global pharmaceutical company dedicated to innovation in health solutions for humans and animals, driven by a diverse workforce of over 53,000.
Ingelheim am Rhein, Rhineland-Palatinate
Our people are our strength. And together with over 54,000 colleagues, we're creating the next breakthrough in the world of healthcare and innovation for both humans and animals. Are you ready to join us? #LifeForward Privacy Notice: https://www.boehringer-ingelheim.com/privacy-notice Imprint: https://www.boehringer-ingelheim.com/imprint
On-site · Brampton
Develop and implement in vitro target engagement, pharmacodynamic, and disease biomarker assays to support immunology and respiratory research. Lead biomarker strategies and provide technical leadership and mentorship within a matrix organization.
On-site · Brampton
Lead global pharmacovigilance and risk management strategies for marketed and investigational compounds. Oversee safety profiles, manage regulatory documents, and lead internal working groups to ensure patient safety.
Hybrid · Brampton
Manages a team of 6-10 reports and a budget of 1M+ Euro to design and operate global and local IT solutions. Focuses on driving innovation and cost efficiencies by creating US-first solutions that can be scaled globally.
On-site · Brampton
Responsible for global pharmacovigilance and risk management activities for marketed and investigational oncology compounds. This includes leading Asset Benefit Risk Teams and representing the company during global health authority interactions.
Hybrid · Burlington
Lead and shape the Regional Operating Unit Medicine Quality Management System to ensure patient safety, data integrity, and regulatory compliance. Manage the QM team, oversee inspections, and drive a culture of continuous improvement and quality across the organization.
On-site · Brampton
The postdoctoral fellow will conduct independent research on controlled API-polymer solidification processes to understand chemical engineering fundamentals. They will also collaborate with a team of experts to present findings and publish research in leading scientific journals.
On-site · Brampton
The Postdoctoral Fellow will design and conduct independent research in clinical pharmacology and pharmacometrics to support drug development. They will collaborate with interdisciplinary teams to analyze data, present findings, and publish research in leading scientific journals.
On-site · Brampton
Lead and develop the Ridgefield Preclinical PKPD Modeling team to drive innovative model-informed decision-making in early drug discovery. Collaborate across global disciplines to deliver translational strategies and human efficacious dose predictions across the portfolio.
Hybrid · Brampton
Lead the strategy and effectiveness of patient support programs, focusing on data analytics, quality monitoring, and performance measurement across the portfolio. Manage patient services vendors and collaborate with cross-functional teams to drive innovation in the patient and HCP experience.
Hybrid · Brampton
Lead the strategy and effectiveness of patient support programs, including data, quality, and performance monitoring across the portfolio. Manage patient services vendors and oversee the modernization of data and analytics roadmaps to improve patient and HCP experiences.
On-site · Brampton
The Vice President leads the therapeutic area clinical development and medical affairs strategy to ensure successful product launch and post-launch performance in the US market. They are responsible for managing cross-functional teams, driving evidence generation, and overseeing medical engagement activities.
Hybrid · Brampton
The Director leads the patient support program strategy, design, and implementation for assigned therapeutic areas. They are responsible for managing external vendor performance, coordinating with cross-functional teams, and ensuring programs meet financial and operational objectives.
On-site · Brampton
You will lead a team of clinical trial experts to drive the planning, execution, and reporting of early-stage immunology clinical trials. Additionally, you will manage resources, budgets, and cross-functional collaborations to ensure operational excellence and adherence to regulatory standards.
Hybrid · Burlington
The specialist ensures the provision of accurate, balanced, and high-quality medical information to healthcare professionals and internal stakeholders. They also mentor the team, manage the medical information website, and participate in medical-legal reviews for compliance.
On-site · Brampton
Lead the strategic oversight of contract compliance for PBM and Maximum Fair Price obligations to safeguard company assets. Manage a team of professionals to ensure accurate rebate processing and optimize Gross-to-Net strategies.
Hybrid · Brampton
Manage the analysis, negotiation, and execution of product discount and rebate agreements to optimize product positioning. Lead the development and implementation of Value Based Contracts in collaboration with cross-functional teams.
Hybrid · Burlington
Provide accurate and high-quality medical information to healthcare professionals and patients while mentoring the Medical Information team. Manage the external MI website and participate in the Medical Legal Review process to ensure scientific accuracy and compliance.
On-site · Brampton
Design and implement end-to-end automated workflows and orchestration platforms for biotherapeutics discovery. This includes developing liquid handler scripts and integrating automation systems with digital data infrastructure.
On-site · Brampton
The scientist will design, execute, and interpret Surface Plasmon Resonance (SPR) experiments to characterize the binding kinetics of biotherapeutic modalities. They will collaborate with cross-functional discovery teams to provide data-driven insights that support lead selection and project progression.
Hybrid · Brampton
Responsible for the review, regulatory assessment, and prioritization of adverse event reports from various sources. Collaborates with cross-functional teams to ensure complete medical information is submitted to health authorities per federal regulations.
