Drug Regulatory Affairs Jobs in Cambridge, MA
Randstad Life Sciences US - Cambridge, MA, United States
Minimum 3 years of PM experience leading complex pharmaceutical projects in a multi-disciplinary, global environment PM experience in Medical Affairs, Clinical Research, Regulatory, CMC, Marketing or other
from: linkedin.com - 5 days ago
Infotree Global Solutions - Cambridge, MA, United States
environment Knowledge of pharmaceutical industry and Project management experience within Medical Affairs, Clinical Research, Regulatory, CMC, Marketing or other drug development related function Experience
from: linkedin.com - 5 days ago
Editas Medicine - Cambridge, Massachusetts
and advanced degree preferred with a minimum of 10 years’ experience in drug development/regulatory affairs and a minimum 8 years in CMC regulatory affairs. Experience with both US FDA and EMA with drugs
Register your RESUMEfrom: resume-library.com (+1 source) - Yesterday
ONO PHARMA USA - Cambridge, MA, United States
and management experience in the PV, Regulatory Affairs department of an established United States-based pharmaceutical company, having worked directly with the Food and Drug Administration (FDA) to successfully
from: linkedin.com - 6 days ago
Bicycle Therapeutics - Cambridge, MA, United States
A thorough understanding of global drug development functional areas including preclinical, clinical, regulatory affairs and manufacturing Highly collaborative, strong relationship building skills with high
from: linkedin.com - 14 days ago
LanceSoft Inc - Cambridge, Massachusetts
Research, Regulatory, CMC, Marketing or other drug development related function Knowledge of the drug development and commercialization process and an understanding of the functions within the pharmaceutical
Register your RESUMEfrom: resume-library.com - 6 days ago
Randstad - cambridge, massachusetts
Medical Affairs, Clinical Research, Regulatory, CMC, Marketing or other drug development related function Knowledge of the drug development and commercialization process and an understanding $85 - $94.21 per hour
from: randstadusa.com (+1 source) - 7 days ago
The Fountain Group LLC - Cambridge, Massachusetts
, Clinical Research, Regulatory, CMC, Marketing or other drug development related function Description: As part of the GMSO Program Management team, you will report to the Strategy & Operations Lead
Register your RESUMEfrom: resume-library.com - 6 days ago
Life Science People - Boston, MA, United States
with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and applicable regulatory requirements. Collaborate with regulatory affairs team to prepare and submit regulatory
from: linkedin.com - 12 days ago
Proclinical Staffing - Boston, MA, United States
including significant experience in senior strategic role, including specific oncology investigational product experience The Senior Director, Regulatory Affairs will: Integrate strategic regulatory & drug
from: linkedin.com - 13 days ago
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