Senior Regulatory Affairs Consultant / Regulatory Project Lead
Billerica, Massachusetts
Parexel International Corporation
If you are passionate about innovative therapies, love leading complex regulatory filings, and live for quality, on time, and within budget project deliverables, Parexel is E-X-P-A-N-D-I-N-G and we currently have openings for Senior Regulat...
13d
| Job Type | Full Time |
King of Prussia, Pennsylvania
Parexel International Corporation
The Manager within R&A provides leadership and direction to Associates, Consultants and Senior Consultants, actively managing employee performance and development. Additionally acts as a role model and provides or organizes coaching/mentori...
13d
| Job Type | Full Time |
Fort Detrick, Maryland
Regulatory Affairs Manager Job Locations US-MD-Fort Detrick Job ID 2025-12321 # of Openings 1 Category Engineering Overview LMI is seeking an experienced Regulatory Affairs Manager to support the Office of Human and Animal Research Oversigh...
13d
| Job Type | Full Time |
Senior Director, Brands Regulatory Affairs
Mylan Inc. At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live health...
13d
| Job Type | Full Time |
Senior Regulatory Affairs Manager
Bedford, Massachusetts
Job Information Number ICIMS-2025-8397 Job function QA&RA Job type Full-time Location Bedford - 180 Hartwell Road Bedford, Massachusetts 01730 United States Country United States Shift 1st About the Position Introduction Werfen Werfen is a ...
13d
| Job Type | Full Time |
Executive Director, Regulatory Affairs Strategy
Cambridge, Massachusetts
Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more t...
13d
| Job Type | Full Time |
Director, RNAi Global Medical Affairs Lead
Cambridge, Massachusetts
Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more t...
13d
| Job Type | Full Time |
Associate Director, Global Pharmacovigilance Quality Management
Cambridge, Massachusetts
Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more t...
13d
| Job Type | Full Time |
Director of Regulatory Affairs CMC
Cambridge, Massachusetts
Who is BlueRock? BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique cell+gene platform to direct cellular differentiation and genetically en...
13d
| Job Type | Full Time |
Cincinnati, Ohio
FDA Regulatory Expert Job Locations United States | United States-OH-Cincinnati Category Regulatory Affairs Job Summary Our clinical and regulatory activities are growing, and we are currently seeking a full-time FDA Regulatory Strategist t...
13d
| Job Type | Full Time |