Drug Regulatory Affairs Jobs in Rahway, NJ

1 to 10 of 21 vacancies

Sort by:  Date | Relevance

Principal Scientist, Clinical Research, Breast Cancer  

Merck - Rahway, NJ 07065

closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and Assist the Senior/Executive Director

from: Pharmadiversityjobboard.com - 20 days ago

Director (Principal Scientist), Regulatory Affairs Liaison- Vaccines and Infectious Disease (Hybrid)  

Merck - Rahway, NJ 07065

committee. Coordinates interactions with foreign agencies through Regulatory Affairs Europe and the subsidiary registration departments to support their interactions and provide strategic direction across

from: Pharmadiversityjobboard.com - 18 days ago

Senior Regulatory Affairs Associate  

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 - 12 days ago

Principal Scientist, Clinical Research, Thoracic Malignancies  

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 - 30 days ago

Senior Principal Scientist, Clinical Research, Hematology/Lymphoma  

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

Safety Case Management Product Specialist  

GForce Life Sciences - Princeton, NJ, United States

preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual

from: linkedin.com - 7 days ago

Program Manager, Clinical Database Services  

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

Senior Medical Director, Oncology Asset Development Team  

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

GPV Submission Specialist  

GForce Life Sciences - Princeton, NJ, United States

preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual

from: linkedin.com - 9 days ago

Register your RESUME
Post your RESUME now with our Partner
and receive job offers perfect for you!

Senior Clinical Director  

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


Get email alerts for: Drug Regulatory Affairs Jobs in Rahway, nj

Top locations

Loading map...

Top locations near Rahway, NJ hiring now Drug Regulatory Affairs Jobs:

Login through

JobisJob Tutorial

Visit our Help Centre

JobisJob Forum

Start a Discussion and Share your Insights.

Join

Share Options

Filter jobs by

Refine your search