3 intern jobs found in Boston

Biogen About the Role: This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. Biogen's Health Literacy & Plain Language Center of Excellence (CoE) is seeking a motivated intern in to support various initiatives designed to transform Biogen into a "health literate" organization that disseminates consistent, understandable, and accessible messaging to our patients and the public. The intern selected for this opportunity will learn and apply health literacy and plain language principles to real projects, gaining practical experience in translating complex, scientific jargon into understandable, patient-forward messaging. The intern will also have the opportunity to learn about the various parts of the clinical trial process, how Biogen conducts clinical trials, and will also gain exposure to collaboration across different functions in clinical operations. In this role, the intern will also learn the essentials of...

Biogen This is a remote position that requires the candidate to be located in the United States. About this role The Senior Principal Analyst, Statistical Programming leads and oversees statistical programming activities of internally and externally through vendors in the application of data standards, production of analysis datasets, analysis dataset specifications, tables, listings, figures, electronic submission components (define.xml and XPTs), and ad hoc analyses. He/She partners with Biostatistics to deliver high quality, submission ready statistical outputs. This person is also responsible for providing input to the Statistical Programming Portfolio Lead (PL) on overall study timelines, monitoring and meeting agreed upon program(s) milestones, escalating issues as needed to their DM counterpart and estimating resources needs. He/She leads a drug program team of statistical programmers to accomplish tasks and communicate issues, as necessary, to senior management....

Biogen About This Role This role is part of the Clinical Trial Accelerator Unit (CTAU) and is responsible for accelerating Study Start Up activities and ensuring all site activations are made on time in global clinical studies. The individual will harmonize processes and provide start-up expertise to assigned studies and programs, ensuring study teams meet or exceed Final Protocol to First Patient In timelines. The role involves direction and execution, quality compliance, risk management, performance monitoring and cross-functional collaboration. What You'll Do Lead and oversee the execution of site activation for global clinical studies Develop and maintain critical path and timelines for site activation Oversee and negotiate timelines for Master Informed Consent Forms (ICFs), including country and site-level ICF creation. Ensure site activation activities are inspection-ready and compliant with ICH-GCP and Biogen SOPs Perform or delegate quality checks on...