About This Role
In this role, you will join our safety surveillance team and play an integral part in advancing therapies that enhance the health and quality of life for patients. You will work in a dynamic global biotech environment, gaining hands‑on experience in safety assessments of treatments to ensure they meet the highest standards.
This position is a 12‑month fixed‑term contract, starting in the summer of 2026. It 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 can work independently while following instructions and guidance, and you are resourceful, collaborating across various departments globally. Detail orientation is second nature to you, ensuring accuracy in reports and data analysis even with competing priorities, and your communication is clear and unambiguous.
Required Skills
* A recent postgraduate degree in life sciences such as Biomedical Sciences, Biochemistry, Biosciences, or an 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.
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