innovative biotechnology product candidates across multiple therapeutic areas. Further information about AlexionPharmaceuticals...Location: Onsite at either, Boston -Seaport, Cambridge, MA or New Haven, CT. Alexion (AstraZeneca Rare Disease...
Some opportunities happen only once in a lifetime - like a job where you have the chance to change lives. At Alexion...: The Alexion IT organization is seeking an Associate Director, IT Business Partner to join their US Commercial IT team...
studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local... feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion...
of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard... Alexion rare disease areas. Ability to work in an environment of remote collaboratorsand in amatrix reporting structure...
The Sr. Manager, R&D Resource Management, is a pivotal role at the intersection of several functions. The successful candidate will support the resource capacity planning process, an essential component for the Long-Range Plan, R&D prioriti...
program lifecycle at Alexion. Accountabilities Lead quality for end-to-end clinical product release, ensuring timely... office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca's Alexion...
This is what you will do: The Manager, PRC Coordinator, Promotional Review and Operations (PRO) is a dynamic leader responsible for managing and optimizing the promotional review process for commercial advertising within the designated th...
for consideration Act as liaison between KOLs and Alexion for on-label activities, including office-based cross-functional colleagues... office while respecting individual flexibility. Join us in our outstanding and ambitious world. At AstraZeneca's Alexion...
Seeking a physician with 3-5 years of clinical research or clinical trials experience in industry or equivalent experience in academia or hospital system. The primary role is to work within the Hematology/Nephrology Clinical Development Dep...
This is what you will do: Position Summary The Manager of Global Regulatory Affairs Chemistry, Manufacturing, and Controls (GRA-CMC) will support project teams and complex projects for compiling global CMC submissions and responses to r...