The Senior Professional Services Veterinarian provides technical education and sales support to internal personnel and external veterinary customers. They are responsible for implementing training initiatives, managing key opinion leader relationships, and ensuring the technical accuracy of promotional communications.
The Senior Global Medical Advisor designs the global medical affairs strategy for oncology compounds and leads strategic initiatives to ensure successful commercialization. They act as the medical ambassador for the asset, overseeing evidence generation and engaging with internal and external stakeholders.
Develop and execute U.S. public policy and advocacy strategies for biomedical innovation, clinical research, regulatory science, emerging technologies, and the broader science ecosystem. Advise senior leaders, coordinate cross-functional initiatives, develop policy positions and executive communications, and represent the company with external stakeholders.
The Associate Director will devise and execute document strategy for clinical development programs while independently writing and managing key global clinical documents. They will also oversee internal and external medical writers, contribute to process improvements, and represent the function in cross-functional working groups.
The fellow will integrate multimodal data to build and validate clinical trial simulation models for operational and clinical decision support. They will also develop reproducible simulation pipelines and communicate statistical findings to cross-functional stakeholders.
Lead global regulatory strategy for assigned products throughout development and lifecycle management, assessing regulatory risks and opportunities and guiding submissions, labeling, and health authority interactions. Lead and mentor the Regulatory Excellence Team, represent Global Regulatory Affairs on Evidence Teams, and align regulatory plans with product development and business objectives.
Lead legal counsel for the 340B function and advise Value & Access teams on government pricing, federal healthcare programs, compliance, competition law, and payer and trade matters. Provide strategic advice to senior leaders, negotiate complex agreements, supervise outside counsel as appropriate, and mentor junior legal and department staff.
The Director, Senior Clinical Program Leader provides strategic and medico-scientific leadership for clinical programs to accelerate development and achieve regulatory approvals. They are responsible for managing cross-functional evidence teams, overseeing clinical trial protocols, and ensuring continuous benefit-risk assessment throughout the development lifecycle.
The Director, Senior Clinical Program Leader provides medico-scientific and strategic leadership for clinical programs to accelerate development and achieve regulatory approvals. They are responsible for the execution of clinical development strategies, risk/benefit oversight, and leading cross-functional evidence teams.
Lead proactive patient safety and benefit-risk strategies for investigational compounds throughout early clinical development. Collaborate with cross-functional teams to oversee safety surveillance, signal evaluation, and regulatory documentation.
Lead proactive patient safety and benefit-risk strategies for investigational compounds throughout early clinical development. Collaborate with cross-functional teams to oversee safety surveillance, signal evaluation, and regulatory documentation.
The consultant will build relationships with swine farmers and veterinarians to promote products and provide value-added solutions. They are responsible for achieving sales targets within their assigned territory while maintaining strong connections with key stakeholders.
The Patient Safety Physician is responsible for global pharmacovigilance and risk management activities for marketed and investigational compounds. They lead cross-functional asset benefit-risk teams and represent the company in interactions with global health authorities.
The Senior Category Manager shapes global sourcing strategies for clinical trials and manages relationships with core service providers. They are responsible for identifying market enhancements, negotiating contracts, and leading cross-functional teams to improve cost efficiency and value generation.
The consultant is responsible for executing brand strategies and driving sales growth for cardio-renal-metabolic products within targeted healthcare accounts. They will engage with healthcare providers using both in-person and digital platforms to deliver clinical value and support patient care protocols.
The fellow will integrate multimodal data to build and validate clinical trial simulation frameworks that quantify operational and clinical risks. They will also develop reusable simulation pipelines and communicate findings to cross-functional stakeholders to support trial design decisions.
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.
