63 jobs found in Rowley, MA

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 the Role: This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. This role is looking for 3 interns. The Biostatistics Department in the Statistical Sciences & Evidence Generation organization provides statistical support across Research and Development. Biostatisticians in the Biostatistics Department collaborate with stakeholders from different disciplines to develop agile and robust clinical development plans and decision frameworks for a portfolio of products encompassing early and late-stage development. They also provide statistical expertise and manage the activities for clinical programs to ensure valid and efficient study designs. What You'll Do: For the summer intern projects, you will be required to read and synthesize key methodology papers, efficiently develop analysis/simulation code in R or python or another statistical package, and explore results in a systematic way. Any new...

Biogen About This Role Pharmacometrics analyses and insight are critical in the development of drug candidates, determination of product viability, and maximization of commercial value at Biogen. As the Associate Director, Pharmacometrics, you will provide pharmacometrics expertise for high-priority clinical development programs and support quantitative decision-making through advanced modeling and simulation. In this role, you will contribute to the pharmacometrics strategy across disease areas and serve as a key scientific resource to program teams and functional partners. You will report to the Head ofPharmacometrics and collaborate closely with cross functional teams to ensure pharmacometrics analyses are appropriately applied to program needs. What You'll Do Provide pharmacometrics expertise to activities throughout the drug development lifecycle and effectively collaborate with cross functional teams Execute advanced pharmacometrics analyses, with emphasis on...

Biogen About This Role: As a Senior Manager in IT Commercial Data Management, you will play a vital role in enhancing our data capabilities across the organization. Working closely with Enterprise IT and Business Stakeholders, you will lead pivotal initiatives that span Snowflake cloud data engineering, data product ownership, and data quality. This position requires hands-on involvement in daily engineering activities while driving strategic data projects. You will manage data-sharing and analytics as an IT Product Owner, develop innovative data products, and implement data governance across our alliance partnership. Your efforts will directly support our US Analytical teams, offering insights into HCP preferences, engagement, and channel effectiveness, thereby adding significant value to the business. This individual should have the ability to work eastern standard hours. What You'll Do: Serve as IT Product Owner, managing data-sharing and analytics with alliance...

Biogen About This Role The (Senior) Study Data Tabulation Model (SDTM) Programmer will be part of the SDTM Development and Operations organization that is evolving and responsible for fulfilling all of Biogen's SDTM needs with presence in the Unites States and Europe. What You'll Do You will lead study level SDTM programming activities and deliverables (annotated Case Report Form (aCRF), specifications, datasets, define.xml, Study Data Reviewers Guide, etc.). Collaborating cross-functionally within Analytics and Data Science, you will work other study leads within the Biometrics organization to ensure timely and quality SDTM deliverables for the study. You will represent SDTM Development and Operations (Dev & Ops) in the Biogen Portfolio Disease Unit (DU) discussions. You will ensure quality SDTM package delivery to the Statistical Programming group through programming and oversight of the study SDTM activities. Who You Are You are a Clinical SAS...

Biogen About This Role: As Biogen's Access Management Service Delivery Manager (SDM) you are the Access Management subject matter expert and services leader for all Access Management activities at Biogen. This role is accountable for delivering value to global stakeholders - which includes access services to every application in Biogen. A peer to this role is the Service Delivery Manager of Identity. This role is a direct report of the Global Leader of Identity and Access Management and is a member of the extended leadership team within the Cybersecurity organization. As Access Management SDM, you are responsible for establishing access management policies and standards and keeping them current. You are responsible for the planning and execution of initiatives that improve access management capabilities - both central platforms or efforts supporting independent stakeholder applications. This role is responsible for the entire service delivery process, from planning and...

Biogen About This Role: As a Senior Pharmacovigilance (PV) Lead, you will provide strategic and operational PV/safety support for Biogen's West Coast Hub development programs, working closely with cross-functional colleagues. This Director level position is pivotal in overseeing global safety operations, ensuring high-quality pharmacovigilance deliverables, and offering expert guidance across the organization. You will manage internal and external PV resources, lead cross-functional safety governance, and serve as a subject matter expert for safety strategy across clinical development, regulatory filings, and post-marketing activities. This role is integral to the business structure, fostering collaboration and advancing the strategic safety objectives of the organization. What You'll Do: Manage internal PV personnel and external resources, including full oversight of all PV vendor activities to ensure operational excellence and compliance. Build (where applicable) and...

Biogen About This Role Biogen's West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey. As the Lead, Clinical Pharmacology, Immunology, you will serve on program and study teams, providing strategic leadership in the development and execution of clinical pharmacology plans for drug candidates. You will integrate knowledge of clinical and quantitative pharmacology to optimize and provide rationale for dosage regimens, and study designs throughout the drug development lifecycle. This position is located in South San Francisco office or could be fully Remote. The candidate must reside within the USA. What You'll Do Provide clinical pharmacology expertise to program and study teams throughout a molecule's lifecycle (discovery through...

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 About This Role: The Global Clinical Supply Chain (GCSC) organization plays a critical role in delivering medicines to patients participating in Biogen's clinical studies worldwide. As we advance toward Vision 2030, GCSC is modernizing how we work-simplifying processes, embracing digital and AIenabled workflows, and building a workforce ready for the future. The Process Capabilities & Governance Lead is a highly visible, strategic individual contributor role at the center of this transformation. This role exists to modernize GCSC's ways of working, unlock sustainable productivity gains, and reduce friction across complex, crossfunctional operating models. You will define how processes are governed, changed, measured, and continuously improved across GCSC-while also helping the organization adopt digital, automation, and AIenabled workflows. Just as importantly, you will help upskill the workforce to thrive in a datadriven, digitally enabled environment....

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Head of PV Science, the Associate Director, Drug Safety and Pharmacovigilance Scientist is responsible for assessing and interpreting safety data from multiple sources, including clinical trials, spontaneous and solicited reports, aggregate, and literature reports. This individual is expected to provide interpretation and summaries of drug safety information and provide input in the generation of safety reports (e.g., DSURs, PADERs, PBRERs, and clinical safety assessments). This individual may also support the medical assessment of Individual Case Safety Reports...

Biogen About the Role: This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. As an intern, you will work at the intersection of research, analytics, and strategy, partnering closely with experienced data scientists, analytics leaders, and business stakeholders. You will help frame complex questions, design and test advanced models, and translate results into clear, actionable insights. This role offers a highly collaborative environment and exposure to highimpact problems while allowing room for academic rigor, experimentation, and learning. What You'll Do: Assist in end-to-end delivery of data science insights, from framing the business question, designing the solution, and delivering recommendations. Collaborate within the insights & analytics team, coordinating efforts with counterparts to develop and execute a comprehensive brand analytics plan. Deliver consolidated insights and actionable...

Biogen About this role The Medical Science Liaison / Senior Medical Science Liaison (MSL) role is a part of US Medical Affairs, a strategic partner within Biogen, that helps inform medical practice across our therapeutic areas and pipeline to improve meaningful patient outcomes. The MSL enables critical stakeholder engagement with Key Medical Experts (KMEs) and other healthcare professionals (HCPs) so they understand the clinical and scientific narrative for Biogen's therapies. Biogen's priority is to continue to foster and enable a diverse and inclusive workforce - representing age, gender, sexual identity, race, ethnicity, Veterans, and people with disabilities - that reflects the communities where we operate and the patients who we serve. This territory will cover MO, KS, NE, ND, SD, MN, IL, WI, and IA. The successful candidate must reside within the boundaries of the territory. What You Will Do Be a credible medical/ scientific expert who engages with KME and...

Biogen About This Role Biogen is seeking a Director to serve as the value evidence strategic lead for our innovative pipeline. This individual will lead the strategic development and execution of payer-focused evidence generation plan (e.g. real-world evidence, health economic modeling, systematic literature reviews and patient-reported outcomes) for one or more assets or therapeutic indications. A strategic mindset and technical expertise, along with the ability to work closely with alliance partners, are critical! The role will report directly to the Head of Value Evidence Strategy within the broader Value & Access team. What You'll Do Provide high-impact strategic decision-making on key value evidence priorities Provide external thought leadership on value demonstration approaches Interface with cross-functional partners to ensure alignment on value evidence strategy Represent Biogen's perspectives on value demonstration with key alliance partners Lead...

Biogen About this role The Field Director, Medical Science Liaisons is a leadership role within US Medical Affairs and a strategic partner across Biogen. This role provides leadership, strategic direction, and operational excellence to a regional team of Medical Science Liaisons (MSLs), ensuring the effective translation and execution of medical strategy in support of meaningful patient outcomes. Biogen's priority is to continue to foster and enable a diverse and inclusive workforce - representing age, gender, sexual identity, race, ethnicity, Veterans, and people with disabilities - that reflects the communities where we operate and the patients who we serve. What You'll Do Strategic Planning & Execution Collaborate with Global Medical Directors, US and global brand teams, clinical partners, and crossfunctional stakeholders to develop and implement regional field medical strategies, translating enterprise and brand objectives into clear, actionable plans...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: The Senior Director, Clinical Pharmacology will lead Nuvalent's clinical pharmacology strategy across all development programs, including latestage registrational efforts and emerging earlyphase assets. This leader will guide dose optimization, exposure-response modeling, regulatory strategy, and clinical pharmacology components of NDA submissions. Responsibilities: Serve as the clinical pharmacology lead and develop and execute strategies to support Phase 1, registrational, and postmarketing studies, including designing and leading clinical pharmacology studies. Drive the...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role The Senior Director, DMPK will serve as the company's key expert overseeing DMPK strategy across the entire company, including late-stage discovery, development, NDA submission, and commercial readiness, as well as designing, implementing, and interpreting DMPK studies, ensuring high-quality data and regulatory-ready documentation to support IND, CTA, and NDA filings. As part of a growing biotech organization, the role requires a hands-on, collaborative leader who can build and guide a high-performing team while working cross-functionally to advance a dynamic portfolio. This is a...

Biogen About This Role Corporate Development leads the establishment of Biogen's corporate strategy and is responsible for the identification, assessment and negotiation of external opportunities to augment Biogen's pipeline, as well as integration of acquired companies and management of relationships with Biogen's partners. The Search & Evaluation Director for Neuroscience will be contributing to the search and evaluation process to proactively identify and scientifically/technically evaluate external growth opportunities for inbound partnering (e.g., collaborations, licensing, and M&A). In addition to playing an important role in expanding Biogen's pipeline, the Search and Evaluation Director will have the opportunity to contribute to identifying and defining Biogen's strategy in Neurology and Neuromuscular Diseases. What You'll Do Work closely with Corporate Strategy and R&D Leadership to clearly understand the external business strategy and search...

Biogen Job Description About This Role: The Senior Manager, Global Insights will partner with the Global Insights Leads for Nephrology in delivering high-quality insights and forecasting to inform strategic and operational decisions across the nephrology portfolio. This role will focus on generating actionable insights from multiple data sources, supporting market research, competitive intelligence, and forecasting activities. The individual will collaborate closely with cross-functional teams and global/local stakeholders to ensure insights are effectively translated into business strategies. The position requires strong analytical skills, strategic thinking, and the ability to synthesize complex data into clear recommendations. What You'll Do: Analyze and interpret diverse data sources, transforming them into valuable insights to understand customer groups, market trends, and business opportunities. Utilize advanced statistical methods and predictive modeling to...

Biogen About This Role The Associate Medical Director, Scientific & Value Communications role is a part of the US Medical Affairs team, acting as a strategic partner that helps inform medical practice across the Rare Disease therapeutic area to improve meaningful patient outcomes. Through development, support and execution of a cross-functionally accepted Scientific Communication Plan, the Associate Medical Director, Scientific & Value Communications will ensure consistent, compliant and impactful communications via publications, congress activities and medical education. This individual contributor role supports Rare Disease and reports to the Head of Scientific & Value Communications, US Medical Affairs. What You'll Do Contribute to the development of successful and compliant execution of the Scientific & Value Communications strategy, including publications (abstracts, posters, manuscripts), congresses (medical booth, symposia), digital content,...