Alnylam is the world's leading RNA interference (RNAi) company.
Founded in 2002, Alnylam was built upon a bold vision of turning scientific possibility into reality by harnessing the power of RNAi for human health as an innovative new class of medicines. We are a growing biopharmaceutical company with three approved medicines and a robust pipeline of investigational medicines focused in four strategic therapeutic areas: genetic medicines, cardio-metabolic diseases, infectious diseases, and central nervous system (CNS) and ocular diseases, including several in late-stage development.
Headquartered in Cambridge, Mass., Alnylam employs over 1,500 people in 19 countries and is rapidly growing globally, with additional offices in Norton, Mass., Maidenhead, U.K., Zug, Switzerland, Amsterdam, Netherlands, and Tokyo, Japan. Alnylam is proud to have been recognized as one of The Boston Globe's Top Places to Work six years in a row (2015-2020), a Great Place to Work in the U.K. and Switzerland two years in a row (2019-2020) and a Science Magazine's Top Employer two years in a row (2019-2020). Please visit www.alnylam.com for more information.
The Associate Director, Launch Excellence will help drive the US launch readiness and execution for vutrisiran to treat the polyneuropathy of hATTR amyloidosis, as well as prepare the organization for the expansion of the TTR franchise into hATTR-cardiomyopathy. This role is the center point for commercial launch readiness and execution and will partner with the US Brand Lead and cross-functional Brand Team to manage and execute the vutrisiran launch. The role will also partner closely with the global launch excellence lead for TTR to ensure US and global preparation and activities are in sync.
Responsibilities for this role include leading and tracking all US launch planning and execution (including managing communication, cross-functional interdependencies, and timelines) for vutrisiran in the US. The role will report to the Director, Launch Excellence and is based in Cambridge, MA.
Summary of Key Responsibilities
Provide support and guidance to the vutrisiran MAC Team leads (Marketing, Medical Director, and Market Access) to set agenda and priorities for biweekly meetings, make recommendations on topics and time allotments, and generally help prepare them for MAC Team meetings.
Support US vutrisiran MAC Team in execution of US launch.
Drive efforts across all other functions (Training, Manufacturing, Market Research, Forecasting, Business Insights, IT/CRM, Patient Services, Patient Advocacy, Public Affairs, Field Force, Finance, Distribution, Drug Safety, etc.) to ensure alignment and compliance with planned timelines and execution plans. Gain commitment and ensure accountability from functional leads related to launch planning and execution.
Identify and prioritize projects with significant impact on launch success and support effective tactical implementation where appropriate.
Provide Launch Excellence input and support to Brand Planning and Investment Planning process.
Ensure launch plans are updated in a timely manner by all functions, and information is accessible to all appropriate team members.
Escalate issues as appropriate, to drive toward resolution. Ensure transparency.
Support scalable development of launch capabilities, technology, and business process as appropriate.
Qualifications
Education (Minimum) Requirements: Bachelor's degree; Ph.D. or MBA is preferable
7 years of biopharmaceutical experience; particularly in Commercial, Marketing or Operations roles
2 years project management experience, including managing cross-functional teams and/or external partners through large, complex projects or initiatives
Consulting experience preferred
Excellent interpersonal skills with a track record of effectiveness and collaboration as a team player and result-oriented project leader
Superb written and verbal communication skills, including ability to present to senior management
Experience with the technology and tools used to manage complex programs (e.g. Smartsheet, PowerPoint, Excel, etc)
Ability to handle multiple projects simultaneously to meet tight deadlines
Strong leadership and decision-making skills
Ability to work independently
Flexibility and ability to adapt to changing conditions
Self-starter who demonstrates energy and enthusiasm, bringing a positive can-do approach to all challenges
Experience in specialty/rare disease markets preferred
Experience in a US role is preferred
Demonstrated ability to analyze large amounts of information and extract insights
Ability to develop strong, professional relationships
Alnylam Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment.
Associate Director, Launch Excellence
Overview
Alnylam is the world's leading RNA interference (RNAi) company.
Founded in 2002, Alnylam was built upon a bold vision of turning scientific possibility into reality by harnessing the power of RNAi for human health as an innovative new class of medicines. We are a growing biopharmaceutical company with three approved medicines and a robust pipeline of investigational medicines focused in four strategic therapeutic areas: genetic medicines, cardio-metabolic diseases, infectious diseases, and central nervous system (CNS) and ocular diseases, including several in late-stage development.
Headquartered in Cambridge, Mass., Alnylam employs over 1,500 people in 19 countries and is rapidly growing globally, with additional offices in Norton, Mass., Maidenhead, U.K., Zug, Switzerland, Amsterdam, Netherlands, and Tokyo, Japan. Alnylam is proud to have been recognized as one of The Boston Globe's Top Places to Work six years in a row (2015-2020), a Great Place to Work in the U.K. and Switzerland two years in a row (2019-2020) and a Science Magazine's Top Employer two years in a row (2019-2020). Please visit www.alnylam.com for more information.
The Associate Director, Launch Excellence will help drive the US launch readiness and execution for vutrisiran to treat the polyneuropathy of hATTR amyloidosis, as well as prepare the organization for the expansion of the TTR franchise into hATTR-cardiomyopathy. This role is the center point for commercial launch readiness and execution and will partner with the US Brand Lead and cross-functional Brand Team to manage and execute the vutrisiran launch. The role will also partner closely with the global launch excellence lead for TTR to ensure US and global preparation and activities are in sync.
Responsibilities for this role include leading and tracking all US launch planning and execution (including managing communication, cross-functional interdependencies, and timelines) for vutrisiran in the US. The role will report to the Director, Launch Excellence and is based in Cambridge, MA.
Summary of Key Responsibilities
Provide support and guidance to the vutrisiran MAC Team leads (Marketing, Medical Director, and Market Access) to set agenda and priorities for biweekly meetings, make recommendations on topics and time allotments, and generally help prepare them for MAC Team meetings.
Support US vutrisiran MAC Team in execution of US launch.
Drive efforts across all other functions (Training, Manufacturing, Market Research, Forecasting, Business Insights, IT/CRM, Patient Services, Patient Advocacy, Public Affairs, Field Force, Finance, Distribution, Drug Safety, etc.) to ensure alignment and compliance with planned timelines and execution plans. Gain commitment and ensure accountability from functional leads related to launch planning and execution.
Identify and prioritize projects with significant impact on launch success and support effective tactical implementation where appropriate.
Provide Launch Excellence input and support to Brand Planning and Investment Planning process.
Ensure launch plans are updated in a timely manner by all functions, and information is accessible to all appropriate team members.
Escalate issues as appropriate, to drive toward resolution. Ensure transparency.
Support scalable development of launch capabilities, technology, and business process as appropriate.
Qualifications
Education (Minimum) Requirements: Bachelor's degree; Ph.D. or MBA is preferable
7 years of biopharmaceutical experience; particularly in Commercial, Marketing or Operations roles
2 years project management experience, including managing cross-functional teams and/or external partners through large, complex projects or initiatives
Consulting experience preferred
Excellent interpersonal skills with a track record of effectiveness and collaboration as a team player and result-oriented project leader
Superb written and verbal communication skills, including ability to present to senior management
Experience with the technology and tools used to manage complex programs (e.g. Smartsheet, PowerPoint, Excel, etc)
Ability to handle multiple projects simultaneously to meet tight deadlines
Strong leadership and decision-making skills
Ability to work independently
Flexibility and ability to adapt to changing conditions
Self-starter who demonstrates energy and enthusiasm, bringing a positive can-do approach to all challenges
Experience in specialty/rare disease markets preferred
Experience in a US role is preferred
Demonstrated ability to analyze large amounts of information and extract insights
Ability to develop strong, professional relationships
Alnylam Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment.