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
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On-site · Brampton
The role involves executing disease state awareness initiatives for Obesity and MASH, including managing campaigns, educational programs, and cross-functional team projects. It also requires monitoring market trends, managing brand budgets, and collaborating with internal and external partners to ensure effective tactical implementation.
On-site · Brampton
Lead the web capability roadmap and product ownership for IT Marketing and Sales, managing the delivery of pharmaceutical brand websites. Direct a cross-functional matrixed team to implement AI/ML-driven capabilities and ensure platform compliance with regulatory standards.
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
The fellow will serve as a regulatory affairs representative on the Human Pharma Review Committee, reviewing promotional materials for compliance with the FDCA and FDA guidance. They will also gain broad exposure to various medical functions through rotations across multiple therapeutic areas.
On-site · Brampton
The Vice President, US Asset Lead & Marketing Lead is responsible for driving the commercial brand strategy and successful product launch for a complex multi-asset portfolio. This role involves leading cross-functional teams across medicine, marketing, and value & access to ensure alignment with global and local strategic objectives.
Remote · United States
The role involves designing and executing clinical pharmacology development strategies to support the clinical development of new and approved drugs. The incumbent will act as a clinical pharmacology representative in project teams and engage with regulatory authorities throughout the drug development process.
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.
On-site · Brampton
The Fellow will develop regulatory labeling expertise by drafting and revising product labeling while ensuring alignment with company core data sheets and health authority regulations. They will also chair Product Label Review Team meetings and provide functional support for regulatory submissions and FDA interactions.
On-site · Brampton
The fellow will compile and analyze regulatory intelligence to support US and global regulatory strategies for drug and device development. They will also collaborate with cross-functional teams to provide regulatory context for business decisions and ensure compliance with health authority requirements.
On-site · Brampton
The Principal Scientist will design and perform cell-based and ligand-binding assays to evaluate neutralizing antibodies in clinical samples. They will also oversee experimental designs, manage external CRO relationships, and provide scientific leadership to junior staff.
On-site · Toronto
The Medical Science Liaison will foster scientific dialogue and consensus by building relationships with external stakeholders to support patient treatment decisions. They are responsible for mapping stakeholder networks, executing engagement plans, and providing scientific insights to inform strategic decision-making.
On-site · Brampton
The fellow will manage U.S. package and labeling operations, ensuring compliance with FDA regulations and internal procedures. They will collaborate with cross-functional teams to support the development, review, and implementation of compliant labeling artwork.
On-site · Brampton
The fellow will support clinical trial preparation, conduct, and closeout activities while ensuring compliance with ICH-GCP and regulatory standards. They will also collaborate with cross-functional teams and external experts to manage trial documentation and site relationships.
On-site · Brampton
The fellow will manage regulatory CMC activities, including change management, sNDA submissions, and post-marketing reports to ensure compliance with FDA requirements. They will also act as a company liaison with the FDA and provide strategic regulatory input for marketed products and investigational drugs.
On-site · Brampton
The fellow will contribute to medical activities within Clinical Development and Medical Affairs, including executing brand tactics and engaging with key external experts. They will also provide scientific expertise for promotional materials and manage medical information inquiries to support healthcare professionals.
On-site · Brampton
The fellow will develop regulatory strategy expertise by interacting with cross-functional teams and acting as a liaison with the FDA for assigned projects. Responsibilities include providing strategic input on development, registration, and marketing approval, as well as managing formal submissions and labeling negotiations.
On-site · Brampton
The postdoctoral fellow will develop spatially-defined in vitro models of chronic kidney disease using bioengineering and genomics to identify new therapeutic targets. They will conduct independent research, collaborate with cross-functional teams, and publish findings in leading scientific journals.
Hybrid · Brampton
The role provides scientific and strategic leadership for the BDS Simulation Hub, overseeing the development of scalable simulations to support clinical trial design and decision-making. The incumbent will lead a global team, drive the adoption of reusable simulation tools, and represent the organization in cross-functional and external scientific initiatives.
Hybrid · Toronto
The Medical Science Liaison drives scientific dialogue and establishes peer-to-peer relationships with external stakeholders to educate on diseases and assets. They also generate action-focused insights and collaborate cross-functionally to support clinical development and patient-centric solutions.
