Clinical Regulatory Affairs Director Jobs in Waltham, MA
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
Register your RESUMEfrom: resume-library.com - 3 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
Mantell Associates - Boston, MA, United States
, while planning for global NDAs / MAAs Director of Regulatory Affairs - Requirements: Rare disease experience preferred Oncology experience Oncolytic Virus experience is a plus Extensive knowledge of FDA
from: linkedin.com - 15 days ago
RBW Consulting - Cambridge, MA, United States
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 Affairs. Our client is focused
from: linkedin.com - 23 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
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
Astria Therapeutics, Inc. - Boston, MA, United States
and integrate diverse R&D activities including but not limited to, preclinical research, clinical development, CMC, regulatory affairs, new product planning, business development and finance. The ideal candidate
from: linkedin.com - 20 days ago
Novo Nordisk - Lexington, MA
of clinical trials, the drafting of medical/ scientific documents, safety monitoring, and data analyses. The Medical Director will also assist the Sr. Medical Director in the development and execution
from: Pharmadiversityjobboard.com - 3 days ago
Takeda - Boston, MA, United States
therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Director, Regulatory Affairs
from: linkedin.com - 23 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
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