Drug Regulatory Affairs Jobs in Parsippany, NJ

Tandym Group - Florham Park, NJ, United States

per device safety reporting requirements In-depth knowledge of the Drug Development process, Signal Detection, and Regulatory Affairs In-depth knowledge of Domestic and Global Safety regulations Profound

from: linkedin.com - 12 days ago

Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States

and through strategic partnerships with manufactures from around the world. JOB SUMMARY: The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval

from: linkedin.com - 15 days ago

Merck - Rahway, NJ 07065

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 - 8 days ago

NS Pharma, Inc. - Paramus, NJ, United States

and other health authority guidances/guidelines. Experience in rare disease/accelerated approvals preferred. Regulatory Affairs Certification is a plus.

from: linkedin.com - 12 days ago

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 - 21 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 - 5 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 - 21 days ago

Merck - Rahway, NJ 07065

, the 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 - 8 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

from: resume-library.com - 3 days ago

Merck - Rahway, NJ 07065

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 - 22 days ago