Director Regulatory Affairs Jobs in Cambridge, MA

Accede Solutions Inc - Lexington, Massachusetts

Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health

from: resume-library.com - 6 days ago

Shepherd Regulatory Search - Marlborough, MA, United States

My client seeks a highly motivated Director of Regulatory Affairs to join their growing organization. In this role, you will be responsible for all activities to lead and maintain global regulatory

from: linkedin.com - 6 days ago

AstraZeneca - Waltham, Massachusetts, USA

with unmet needs. We work across our ground-breaking pipeline and the business to get medicines to patients as efficiently and optimally as possible. The Regulatory Affairs Director (RAD) provides strategic

from: Ivyexec.com - 7 days ago

MapLight Therapeutics, Inc. - Burlington, MA, United States

, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You’ll Do: Reporting to the VP, Regulatory Affairs

from: linkedin.com - 17 days ago

Keros Therapeutics - Lexington, MA

Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, race, color...

from: Pharmadiversityjobboard.com - 13 days ago

AstraZeneca - Boston, Massachusetts, USA

of clinical trials in one or more development programs. You will collaborate with colleagues in other functions including Study Physician, Patient Safety, Regulatory Affairs, Clinical Operations, Translational

from: Ivyexec.com - 7 days ago

Merck - Boston, MA

closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Associate Vice-President/Vice

from: Pharmadiversityjobboard.com - 14 days ago

Sobi - Waltham, Massachusetts

Program Leader Clinical Study Manager Medical Director Lead Medical Program Lead Drug Safety Manager and Physician Regulatory Affairs Manager Clinical Pharmacologist Marketing IT QA Patient Access External

from: resume-library.com - 3 days ago

Novo Nordisk - Lexington, MA

, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and external stakeholders including KOLs and Principal Investigators. Essential Functions

from: Pharmadiversityjobboard.com - 3 days ago

Novo Nordisk - Lexington, MA

with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety, Data Management

from: Pharmadiversityjobboard.com - 23 days ago