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Your search generated 197 results
Akebia Therapeutics

Associate Director Regulatory Labeling

Cambridge, Massachusetts

Akebia Therapeutics

Associate Director Regulatory Labeling LinkedIn Twitter Email Message Share Regulatory Affairs Cambridge, MA * ID: 25R-26 * Full-Time/Regular Nearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. At Akebi...

Job Type Full Time
ICON Technology

Senior Regulatory Affairs Project Manager I

Austin, Texas

ICON Technology

ICON is seeking a highly motivated and dedicated Project Manager to work at the intersection of structural design and testing, overseeing the testing process for validation and regulatory acceptance of ICON's breakthrough 3D-printed structu...

Job Type Full Time
ICON Technology

Senior Regulatory Affairs Project Manager I, MILCON

Austin, Texas

ICON Technology

ICON is seeking a highly motivated and dedicated Sr. Regulatory Affairs Project Manager, MILCON to advance regulatory acceptance and business development across federal government and national security sectors, including the Department of D...

Job Type Full Time
GlaxoSmithKline

Vaccines Manager, Global Regulatory Affairs

Rockville, Maryland

GlaxoSmithKline

Job Description Do you have experience in all aspects of a Regulatory Affairs project, supporting technical/ CMC, clinical, nonclinical and procedural aspects of strategy and submissions, but are looking to take this to the next level, supp...

Job Type Full Time
GlaxoSmithKline

Vaccines Senior Manager, Global Regulatory Affairs

Rockville, Maryland

GlaxoSmithKline

Job Description Are you a subject matter expert in technical / CMC and procedural aspects of Global Regulatory Affairs, driven to provide in-depth input into asset specific regulatory strategy on a global scale for clinical/labelling or tec...

Job Type Full Time
ImmunityBio

Regulatory Affairs Program Manager

Summit, New Jersey

ImmunityBio

Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to o...

Job Type Full Time
Exelixis

Regulatory Affairs CMC Director

Alameda, California

Exelixis

SUMMARY/JOB PURPOSE: Provide Regulatory Affairs CMC expertise and leadership for global commercial and development projects. Develop strategic approaches to enable succesful Health Authority submissions and communications. Work closely with...

Job Type Full Time
Exelixis

Regulatory Affairs Strategy Manager (Oncology)

Alameda, California

Exelixis

SUMMARY/JOB PURPOSE: Responsible for managing and maintaining existing Investigational New Drug (IND), Clinical Trial Application (CTA), New Drug Application (NDA), and Biologics Licensing Application (BLA) submissions and preparing amendme...

Job Type Full Time
BlueRock Therapeutics

Director, Regulatory Affairs Strategy

Cambridge, Massachusetts

BlueRock Therapeutics

Who is BlueRock? BlueRock Therapeutics LP is a clinical stage cell therapy harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases. Two of our novel investiga...

Job Type Full Time
Chiesi

Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026

Cary, North Carolina

Chiesi

Chiesi USA Chiesi USA is a specialty pharmaceutical company focused on developing and promoting products for the hospital, adjacent specialty and rare disease markets. We are a B Corp and Benefit company awarded Top Employer status for six ...

Job Type Intern

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