The Technical Services Veterinarian supports sales and marketing by providing technical expertise and product information to veterinarians and key stakeholders. They are responsible for building customer relationships, resolving technical inquiries, and contributing to strategic species-specific business plans.
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.
The Associate Director leads performance governance, data analytics, and insight generation for the Patient Assistance Program to ensure operational transparency and vendor accountability. This role establishes the single source of truth for program performance and provides data-driven recommendations to leadership and cross-functional stakeholders.
The Medical Science Liaison is responsible for conducting high-quality, peer-to-peer scientific exchange with healthcare stakeholders to support Eye Health objectives. They will gather actionable insights, provide disease-state education, and collaborate with internal teams to support clinical development and research.
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 Regional Sales Manager directs the sales team to implement marketing plans and ensure maximum market penetration for equine products. They are responsible for managing sales representatives, overseeing regional business plans, and ensuring consistent application of company policies.
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 role involves conducting advanced analytics to support promotional strategies, marketing mix modeling, and resource allocation within the oncology therapeutic area. It also requires collaborating with cross-functional teams to develop customer targeting, segmentation, and digital activity tracking to drive brand performance.
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 physician will lead pharmacovigilance and risk management activities for marketed and investigational compounds on a global scale. They will chair internal asset benefit-risk teams and represent the company during 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.
