AP

Alexion Pharmaceuticals, Inc.

Verified Job Source

Transforming Lives, Every Day.

Boston, Massachusetts

Biotechnology Research
5,001+ people

About

Alexion, AstraZeneca Rare Disease is focused on pioneering new possibilities for the rare disease community. We are driven by a mission to change what it means to live with a rare disease. A leader in rare disease for more than three decades and today continues to build a diversified pipeline across disease areas with significant unmet need, using an array of innovative modalities. As part of AstraZeneca, Alexion is continually expanding its global geographic footprint to serve more rare disease patients around the world. It is headquartered in Boston, US. Alexion’s pioneering legacy in rare disease is rooted in being the first to translate the complex biology of the complement system into novel medicines. Alexion pushes boundaries to accelerate discovery of life-changing medicines. Headquartered in Boston, Massachusetts, Alexion has offices around the world and continues to expand its reach to benefit more people globally. GL/NP/0116 GL/NP/0095 Community Guidelines: https://bit.ly/39x9gqy

Open positions

Associate Medical Director, Global Drug Safety

Hybrid · Mississauga

The Associate Medical Director manages safety and risk management activities for clinical development projects and marketed products. Key duties include identifying safety signals, conducting medical reviews of ICSRs, and contributing to core regulatory safety documents.

Associate Medical Director, Global Drug Safety

Hybrid

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. This position is accountable for the timely preparation of high-quality regulatory compliant clinical document deliverables f…