AP

Alexion Pharmaceuticals, Inc.

Source d’offres vérifiée

Transforming Lives, Every Day.

Boston, Massachusetts

Biotechnology Research
5 001 personnes et plus

À propos

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

Postes ouverts

Associate Medical Director, Global Drug Safety

Hybride · Mississauga

The role is responsible for preparing high-quality, regulatory-compliant clinical documents and supporting medical writing activities for clinical programs. It involves leading patient safety teams, overseeing compliance with safety policies, and driving cross-functional strategies within the Rare Disease Unit.

Global Patient Recruitment and Engagement Lead (12-month contract)

Hybride · Mississauga

Lead the development and implementation of data-driven patient recruitment and engagement strategies for rare disease studies. Collaborate with cross-functional teams and external vendors to improve the participant experience and meet enrollment goals.

Senior Manager, Digital Analytics

Hybride · Mississauga

Lead digital analytics and performance measurement across multiple US Commercial brands, focusing on websites, paid media, and social channels. Manage the migration from GA4 to Adobe Analytics and develop scalable reporting standards to drive omnichannel decision-making.

Global Study Associate Director

Hybride

When we put unexpected teams in the same room, we unleash ambitious 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. The Global Study Associate Director (GSAD) is a business-critical role whose main accountability is the delivery of clin…

Associate Director, Medical Writing (6 - Month Contract)

Hybride

This is a 6-Month Contract. 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. Introduction To Role Are you ready to lead the charge in crafting high-quality clinical regulat…

Associate Medical Director, Global Drug Safety

Hybride

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…