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The Manufacturing/Engineering Intern will assist in meaningful projects aimed at designing and constructing a biologics manufacturing facility, collaborating closely with the engineering and manufacturing teams throughout the project's phases.
The intern will assist the Supply Chain Department by supporting business operations through digitization and automation. Responsibilities include driving analytical capabilities, developing performance management tools, and strengthening partnerships within the supply chain.
As a Summer Intern in Translational Research, you'll participate in genomic analysis of clinical trial data, collaborate with teams to improve clinical success rates, and develop analytics methods using bioinformatics tools. Responsibilities include data management and vendor meetings, while receiving mentorship throughout the internship.
The Global Lead of HR Systems and Data is responsible for defining, implementing, and managing global HR systems and data initiatives. This role enhances employee experience through effective HR technology strategy, implementation, and governance while driving digital transformation and optimizing HR processes across the organization.
The Senior Manager, Biostatistician oversees statistical activities for clinical studies, develops protocols, statistical analysis plans, and collaborates with vendors and internal teams to ensure quality and compliance in statistical reporting and analysis.
The Associate Director, Corporate Counsel, R&D will provide legal support for clinical research and development, focusing on contracts and regulatory compliance for clinical trials. Responsibilities include drafting contracts, collaborating with cross-functional teams, offering legal counsel on healthcare laws, and supervising Paralegals and outside counsel.
The Senior Manager of Statistical Programming and Data Operations is responsible for vendor oversight, ensuring quality TLFs, and managing CDISC datasets for regulatory submissions. This role involves collaboration with internal staff and statistical programming vendors, overseeing statistical deliverables, and preparing CDISC data submission packages. The manager also conducts programming quality control and supports process improvements.
The Quality Assurance intern will assist with creating and reviewing SOPs, researching QC equipment, and configuring systems such as LIMS, Empower, and ELN as part of the biologics manufacturing facility project.
Senior Research Scientist leading pharmacologic evaluation of cell and gene therapy research projects to ensure success, providing guidance, managing studies, and contributing to non-clinical development.
The Sr. Research Associate will lead pharmacologic evaluation of cell and gene therapy research projects, contribute to non-clinical development, prepare documentation, and stay updated on advanced technologies for research improvement.
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