About This Role
In this role, youll join our safety surveillance team and will be an integral part of advancing therapies that enhance the health and quality of life for patients. Immerse yourself in the dynamic environment of a global biotech company, where youll gain invaluable, hands‑on experience. Your contributions will be crucial to the safety assessments of treatments, ensuring that they meet the highest standards.
This position offers a unique opportunity to work closely with a team of pharmacovigilance scientists, supporting them in a variety of safety evaluation activities. Your efforts will directly impact our mission to deliver safe and effective therapies to patients worldwide.
This role is available on a 12‑month fixed‑term contract, beginning in the summer of 2026 and is a hybrid role, requiring 50% office attendance each week in Maidenhead.
What You’ll Do
* Perform data review, analysis, and interpretation.
* Support routine safety assessment activities.
* Assist in the preparation of reports submitted to regulatory authorities.
* Screen medical literature for pertinent safety information.
* Participate in meetings and discussions to enhance safety strategies.
* Document important safety management decisions accurately.
* Collaborate proactively with other departments as needed.
* Handle general administrative tasks, including scheduling and information management.
* Conduct editorial reviews to ensure grammatical and stylistic consistency.
Who You Are
You are professional and reliable, with a genuine curiosity about making an impact on the safety of medicines for neurological and rare diseases. You possess the ability to work independently while effectively following instructions and guidance. Your resourcefulness allows you to collaborate across various departments globally. Detail orientation is second nature to you, ensuring accuracy in reports and data analysis, even with competing priorities. Your communication is clear and unambiguous.
Required Skills
* A recent postgraduate degree in life sciences such as Biomedical Sciences, Biochemistry, or Biosciences, or MPharm (Pharmacy).
* Proficient computer skills with the Microsoft suite of products, primarily Word, Excel, and PowerPoint.
* Fluent in English, with strong written and verbal communication skills.
Why 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.
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