Senior PV Scientist

reviews and signal detection activities as part of routine pharmacovigilance oversight.Lead signal management activities for assigned products, including detection, tracking, documentation, evaluation, authoring signal evaluation reports, and leading Safety Signaling Team meetings.Manage literature review activities to identify and assess relevant safety information.Oversee aggregate report management, including strategy, review, and finalization of PSURs, DSURs, RMPs, and related safety documents.Prepare clear, scientifically robust responses to safety questions from regulatory authorities.Collaborate with Global Safety Officers and Safety MDs to support investigational programmes, clinical trial activities, and safety committee management.Manage ad hoc safety data analyses and information requests, ensuring timely and accurate outputs.Who You Are:You possess a deep understanding of pharmacovigilance with an ability to interpret and communicate scientific and medical data effectively. You
thrive in collaborative environments, demonstrating leadership and clinical judgment to navigate complex safety data and regulations. Your strong organizational skills enable you to prioritize tasks independently, ensuring that safety processes are managed efficiently and effectively. You are committed to maintaining high standards and ensuring the integrity of clinical trials and marketed products.Required Skills:Advanced degree (PhD, MPH, NP, PharmD, etc.) required.Significant years of pharmacovigilance experience, including aggregate safety reports and safety signal management.Proficiency in interpreting, analyzing, and presenting scientific and medical data.Strong foundation in pharmacovigilance and drug development, including clinical trial and post-marketing safety regulations.Basic knowledge of common data processing software (Excel, PowerPoint, Microsoft Word, Business Objects) and safety database systems.Demonstrated leadership and collaborative skills within team
environments.Preferred Skills:Expertise in global safety regulations and guidelines.Experience in mentoring and managing staff within pharmacovigilance settings.Ability to apply clinical judgment in safety data interpretation.Job Level: ManagementWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the
patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.SummaryLocation: Maidenhead, United KingdomType: Full time