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HilleVax is a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines. Our initial program, HIL-214, is a virus-like particle (VLP) based vaccine candidate for the prevention of moderate-to-severe acute gastroenteritis (AGE) caused by norovirus infection. It is estimated that norovirus causes nearly 700 million cases of illness and more than 200,000 deaths worldwide per year with significant additional economic and social burdens.
We are founded on the legacies of leading vaccine developers that inspire us to have a positive impact on human health and build a company that equalizes opportunity for people around the world by removing barriers of health inequity. Our aim is to have a global impact on human health; we believe the best way to achieve this impact is by developing novel vaccines for severe and life-threatening diseases.
Objectives / Overview:
The Sr Director, Regulatory Affairs is accountable for developing regulatory strategies for norovirus vaccine candidates with an emphasis on European requirements for early and late stage assets. This person will be a key regulatory leader who partners with internal and external stakeholders to achieve successful regulatory filings and approvals in Europe, US and international.
The successful candidate will have significant regulatory experience in vaccine development with a focus on Europe and the US.
Responsibilities:
HilleVax is a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines. Our initial program, HIL-214, is a virus-like particle (VLP) based vaccine candidate for the prevention of moderate-to-severe acute gastroenteritis (AGE) caused by norovirus infection. It is estimated that norovirus causes nearly 700 million cases of illness and more than 200,000 deaths worldwide per year with significant additional economic and social burdens.
We are founded on the legacies of leading vaccine developers that inspire us to have a positive impact on human health and build a company that equalizes opportunity for people around the world by removing barriers of health inequity. Our aim is to have a global impact on human health; we believe the best way to achieve this impact is by developing novel vaccines for severe and life-threatening diseases.
Objectives / Overview:
The Sr Director, Regulatory Affairs is accountable for developing regulatory strategies for norovirus vaccine candidates with an emphasis on European requirements for early and late stage assets. This person will be a key regulatory leader who partners with internal and external stakeholders to achieve successful regulatory filings and approvals in Europe, US and international.
The successful candidate will have significant regulatory experience in vaccine development with a focus on Europe and the US.
Responsibilities:
HilleVax is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We welcome all to apply.
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#J-18808-LjbffrFull Time
$136k-177k (estimate)
04/27/2024
05/12/2024
The following is the career advancement route for Senior Director, Regulatory Affairs positions, which can be used as a reference in future career path planning. As a Senior Director, Regulatory Affairs, it can be promoted into senior positions as a Regulatory Affairs Director that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Senior Director, Regulatory Affairs. You can explore the career advancement for a Senior Director, Regulatory Affairs below and select your interested title to get hiring information.