The Master Planner is responsible for developing short and long-term production plans based on demand forecasts, communicating with departments, managing inventory levels, and ensuring compliance with regulations and company policies. The role includes using SAP for production scheduling and material requirements planning, and producing related reports.

The Associate Director leads complex clinical trials, ensuring delivery of milestones while managing budgets, timelines, and risks across global teams. Key responsibilities include project management, cross-functional team leadership, and maintaining trial integrity and compliance with regulations.

Develop and optimize gene expression switches for gene therapy, screen small molecule libraries, troubleshoot translational challenges, and evaluate switch functionality in different models.

This position focuses on health outcomes research in oncology, requiring the development of research strategies and project management while increasing knowledge in real-world evidence and economic modeling.

Lead teams to deliver large capital projects in healthcare, ensuring compliance, safety, and effective communication with stakeholders. Require 5+ years in project delivery.

The role involves promoting pharmaceutical products, executing business strategies, building customer relationships, and providing product information while maintaining confidentiality and participating in team collaboration.

The Data Architect will design and build data infrastructure to support AI-driven drug discovery, focusing on data models, architectures, and integration strategies.

The Territory Manager role involves enhancing customer experience through healthcare solutions, engaging with doctors and stakeholders, developing sales plans, and achieving sales targets while adhering to compliance guidelines.

The role involves developing synthesis-aware virtual screening workflows for small-molecule drug discovery, integrating various modeling and design strategies.

The HSE Specialist develops and supports safety systems and programs, ensures OSHA compliance, and supports a safe work environment at the RTP site.

The Clinical Study Build Programmer manages clinical trial data systems, ensuring accurate data collection, programming, testing, and compliance with regulatory standards while collaborating across teams for efficient project delivery.

The Senior Consultant supports lab solutions in Global Manufacturing by configuring lab systems, optimizing processes, and ensuring compliance with quality standards while collaborating with internal and external teams.

The role involves drafting and prosecuting patent applications, advising on legal matters, and leading strategies in patent procurement and litigation for pharmaceutical products.

The Senior Director leads device portfolio strategy, investment prioritization, and integration across functions to optimize project returns and guide executive decisions.

The Associate Director will lead IT projects and programs at a manufacturing site, focusing on supply chain, logistics, and finance processes while ensuring alignment and efficiency in execution.

The Territory Manager for GI Specialty will engage with healthcare providers, drive product adoption, and manage account relationships to improve disease management outcomes in gastroenterology.

The role involves leading ADME studies for the development of genetic medicines, collaborating with cross-functional teams, and mentoring junior scientists.

The Director of Medical Affairs is responsible for providing expert medical support, overseeing clinical trial activities, regulatory support, and strategic planning to enhance customer experience in the healthcare sector. This includes interactions with healthcare professionals, medical communications, and market strategies.

Design, develop, and maintain data solutions to ensure data availability and quality for analytics. Build data pipelines, optimize database designs, and perform data integration and transformation.

Lead the early-stage drug discovery community, focusing on user growth, contributor partnerships, and building relationships with biotech stakeholders. Responsible for platform activation and community engagement to accelerate AI-powered drug discovery.