28 results for Regulatory Associate Jobs in Wilmington, MA, US

Associate Director, US Regulatory, Advertising & Promotion (Hybrid Working Model)Position SummaryThe Associate Director, Commercial Regulatory Affairs will report to the Sr. Director and have accountability for review and approval of promotional and medical communications of assigned brand(s). T...

Company OverviewRhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for heal...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you’ll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients...

Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual...

Responsible for the development and submission of regulatory filings for CRISPR/Cas9-based gene therapy projects. Provides CMC strategic leadership for gene and cell therapy products, manages clinical trial applications, interacts with health authorities, and supports manufacturing and analytical de...

Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve m...

Job DescriptionCompany OverviewSince its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglo...

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment ...

The RoleModerna Therapeutics is seeking an Associate Director of Regulatory Strategy to support programs within the oncology franchise to be based in one of Moderna’s US offices. This is a role intended for a forward looking, creative and agile regulatory strategist able to anticipate and address th...

Responsible for leading global regulatory strategy for biomarkers and companion diagnostic tests, developing global filing strategies, and ensuring compliance with global regulatory requirements. Collaborate with cross-functional teams to address Health Authority queries and contribute to clinical t...