Regulatory Affairs Jobs in Cambridge, MA

RBW is partnering with an innovative late clinical-stage, oncology Biotech (140 FTE) in their urgent and business-critical search for a new Senior Director, Regulatory... Read More

About Third Harmonic Bio Third Harmonic Bio is a biopharmaceutical company with a singular purpose: To create a breakthrough treatment for people living with severe... Read More

Regulatory Affairs Director - Permanent - Boston, MA Proclinical is seeking a Regulatory Affairs Director who will be responsible for the development and execution of... Read More

POSITION FEATURES: This is a remote position with 25% travel PURPOSE AND SCOPE: Manages a field team of regulatory compliance employees and provides regulatory expertise... Read More

This position can be fully remote Global Regulatory experience needed. Demonstrated project management experience needed. PURPOSE AND SCOPE: Ensures company products meet... Read More

Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing... Read More

Mantell Associates is currently partnered with an innovative Biotech company, developing much-needed therapies for people with solid tumors/lung cancer and rare endocrine... Read More

Principal Regulatory Affairs Specialist - Surgical The Principal Regulatory Affairs Specialist will play a key role in launching new products and sustaining the current... Read More

The position will provide regulatory expertise and leadership to assure that the company meets its business objectives while complying with the regulatory framework by... Read More

Job Description Job Description Compass Therapeutics, Inc. is a clinical-stage, oncology-focused biopharmaceutical company developing proprietary antibody-based... Read More

Job title: Global Regulatory Affairs Lead Location: Cambridge, MA or Bridgewater, NJ About the job The Global Regulatory Affairs Lead (GRL) is the fully accountable... Read More

At Editas, we're driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs.... Read More

Job TitlePrincipal Regulatory Affairs Specialist, Software Job Description Principal Regulatory Affairs Specialist, Software (U.S. Hub based) Clinical Integration and... Read More

Principal Regulatory Affairs Specialist, Software (U.S. Hub based) Clinical Integration and Insight (CII) is changing the way healthcare is delivered at the point of care.... Read More

Who We Are Verily is a subsidiary of Alphabet that is using a data-driven approach to change the way people manage their health and the way healthcare is delivered.... Read More

This position can be fully remote Global Regulatory experience needed. Demonstrated project management experience needed. PURPOSE AND SCOPE: Ensures company products meet... Read More

The ideal candidate should have US Advertising and Promotion experience. This position can be fully remote. PURPOSE AND SCOPE: Ensures company products meet regulatory... Read More

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... Read More

Qualifications degree or above in a relevant discipline required years of industrial experience in IVD or medical device FDA registration in Chinese preferred Tasks: and... Read More