Clinical Regulatory Affairs Director Jobs in Lexington, MA
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 - 19 days ago
Novo Nordisk - Lexington, MA
with the VP Medical/Scientific Development, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and external
from: Pharmadiversityjobboard.com - 16 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 - 13 days ago
EPM Scientific - Boston, MA, United States
Our client, a clinical stage biotech company, is seeking an experienced and dynamic Director of Regulatory Affairs to join their team. This exciting opportunity offers the chance for someone
from: linkedin.com - 11 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 - 3 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 - 11 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 - 19 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 - 3 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 - 16 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 - 19 days ago
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