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 - 6 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 - 6 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

from: resume-library.com (+1 source) - 2 days ago

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 - 7 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 - 15 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

from: resume-library.com - 7 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) - 8 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

from: resume-library.com - 7 days ago

Inozyme Pharma - Boston, MA, United States

of excellence, collaboration, and continuous learning. Qualifications: 1. Advanced degree (Ph.D., Pharm.D., or equivalent) in life sciences or a related field. 2. Minimum of 6 years of regulatory affairs

from: linkedin.com - 2 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 - 13 days ago