Drug Regulatory Affairs Jobs in Boston, MA
Pharvaris - Boston, MA, United States
Affairs • Knowledge of regulatory drug development • Excellent verbal and written communication and presentation skills (English) • Strong team player and ability to work across functions (matrix regulatory
from: linkedin.com - 3 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 - 16 days ago
Merck - Boston, MA
Scientists in the execution of clinical studies; Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development
from: Pharmadiversityjobboard.com - 19 days ago
PepGen - Boston, MA, United States
+ years of regulatory affairs experience in drug development and product registration activities within the pharmaceutical or biotech industry in multiple phases of development; both big and small company
from: linkedin.com - 17 days ago
Astria Therapeutics, Inc. - Boston, MA, United States
, and enhance strategic relationships with CDMO and other partners to advance Astria’s patient-guided drug development pipeline. Provide strategic and operational oversight, content creation of all regulatory
from: linkedin.com - 16 days ago
Merck - Boston, MA
of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Associate Vice-President/Vice-President in ensuring that appropriate
from: Pharmadiversityjobboard.com - 22 days ago
Astria Therapeutics, Inc. - Boston, MA, United States
Development, Clinical Operations, Regulatory Affairs, Nonclinical Development, Pharmaceutical Sciences, Discovery and Translational Sciences and other functions in driving asset and company strategy to fruition
from: linkedin.com - 17 days ago
Merck - Boston, MA
the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage
from: Pharmadiversityjobboard.com - 20 days ago
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 - 9 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 - 9 days ago
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