Drug Regulatory Affairs Jobs in Princeton, NJ

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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 - 19 days ago

Director of Regulatory Affairs (Labeling)  

BioPhase - Princeton, NJ, United States

by working collaboratively with key internal stakeholders, including but not limited to Regulatory Affairs, Clinical Research, Drug Safety, Quality, Commercial, Medical Affairs, Legal, Manufacturing

from: linkedin.com - 28 days ago

Senior Director, Regulatory Affairs  

Sun Pharma - Princeton, New Jersey, USA

is to provide regulatory affairs strategic leadership for SPARC and supported Sun novel drug development programs. Of each program this position supports, the individual will be responsible for developing

from: Ivyexec.com - 20 days ago

Senior Director, Head of Regulatory Law  

Sun Pharma - Princeton, New Jersey, USA

, regulatory affairs, and business development teams on product development and drug approval pathways, and on R&D and commercial issues. Review marketing and promotional initiatives, programs presenting

from: Ivyexec.com - 20 days ago

Associate Director, US Regulatory Affairs, Advertising & Promotion  

Proclinical Staffing - Plainsboro, NJ, United States

Regulatory Affairs representative, you will work with brand on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies

from: linkedin.com - 2 days ago

Director, Medical Affairs - Dermatology  

Sun Pharma - Princeton, New Jersey, USA

specialists, and field-based MSLs. In conjunction with the aVP, Medical Affairs, leads the Sun Pharma medical department in regulatory interactions, ISS, expert advisory board meetings, external professional

from: Ivyexec.com - 20 days ago

GPV Case Management Product Specialist  

GForce Life Sciences - Trenton, 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 - 19 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 - 22 days ago

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 - 5 days ago

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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 - 4 days ago


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