and other regulatory documents e.g. DSURs, Briefing Documents, etc. · Represents Alnylam in meetings with regulators, Key Opinion Leaders..., partners, and · other stakeholders · Contributes to scientific articles, summarizing data collected in Alnylam trials...
The Global Study Lead (Sr. Manager, Clinical Operations) is responsible for leading the operational planning and execution of global clinical trials from study start-up through closeout. This role provides leadership to cross-functional tri...
Develop and execute trial operational strategies for assigned studies and contribute to broader program-level planning in partnership with the Director and cross-functional stakeholders. Ensure appropriate timely and quality oversight, and ...
## Overview The Associate Director, Brand Marketing will sit within the International Marketing, Rare Diseases team, part of the Global Rare Business Unit (GRBU). This team is responsible for driving the commercialization and overall prod...