Drug Regulatory Affairs Jobs in East Hanover, NJ
Merck - Rahway, NJ 07065
, the Senior Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs
from: Pharmadiversityjobboard.com - More than 30 days ago
Agios Pharmaceuticals - Anywhere, New York, USA
in Regulatory affairs strategy. Strong demonstration of knowledge of drug development, FDA, EMA and ICH guidelines and regulations Excellent organizational and communication skills, both written and verbal
from: Ivyexec.com - 27 days ago
Merck - Rahway, NJ 07065
Team. Strong organizational, time management, and multi-project coordination skills Broad knowledge of Clinical Development and Regulatory Affairs requirements Ability to multi-task, work independently
from: Pharmadiversityjobboard.com - 19 days ago
Merck - Rahway, NJ 07065
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 - 23 days ago
SK Life Science, Inc. - Paramus, New Jersey
experiences, etc. Manage and processing of CMC Team project invoices and internal project budget requests (ARIBA), and monitoring of project financial tracking. Assist and support Regulatory Affairs (RA
Register your RESUMEfrom: resume-library.com - 25 days ago
Merck - Rahway, NJ 07065
with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects. Assist the Executive Director in ensuring
from: Pharmadiversityjobboard.com - More than 30 days ago
Merck - Rahway, NJ 07065
, the Director may: Supervise 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
from: Pharmadiversityjobboard.com - 30 days ago
Daiichi Sankyo, Inc. - Bernards, NJ
experience including experience within Regulatory Affairs Understanding of scientific content and complexities and good knowledge of diagnostic development, including extensive experience of IDE submissions
from: careerbuilder.com - 4 days ago
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