Pharmaceutical Regulatory Affairs Jobs in New Jersey

GForce Life Sciences - Princeton, NJ, United States

experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical

from: linkedin.com - 6 days ago

GForce Life Sciences - Princeton, NJ, United States

experience processing AE/SAE reports, generating narratives, queries, working within safety databases, and experience with regulatory submissions **Relevant experience includes experience in the pharmaceutical

from: linkedin.com - 8 days ago

Johnson & Johnson - Titusville, NJ

with scientific audiences. Up to 20% travel - Domestic & International Preferred: Experience in the pharmaceutical industry Experience in Clinical development, clinical operations, regulatory affairs, or patient USD 157,000.00 - 271,400.00 per year

from: Dice.com - 11 days ago

Proclinical Staffing - Morristown, NJ, United States

Associate Director, US Regulatory Affairs, Advertising & Promotion - Permanent - NJ & MA Proclinical is seeking an Associate Director, US Regulatory Affairs, Advertising & Promotion for a large

from: linkedin.com - 16 days ago

Meet - , NJ, United States

+ years in the pharmaceutical industry required. 4 years in regulatory affairs. Experience with global labeling. Ability to travel up to 10% If you're interested in hearing more about this opportunity

from: linkedin.com - 16 days ago

Bristol Myers Squibb - Princeton, United States

degree (MD, PhD, PharmD, DNP) Minimum 5 years of experience in pharmaceutical industry; prior experience in oncology medical affairs is preferred Demonstrates thorough understanding of medical review

from: jobrxiv.org - 12 days ago

CMK Select - Trenton, NJ, United States

CMK Select, a specialized project management consulting firm dedicated exclusively to the Pharmaceutical / Life Sciences industry is hiring a skilled Medical Affairs Program Manager to oversee

from: linkedin.com - 15 days ago

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

regulatory affairs operations. Knowledge of eCTD publishing systems and standards, EDMS technology and related publishing tools. Working knowledge of US FDA (OGD/CDER) e-submission requirements. Strong written

from: linkedin.com - 15 days ago

Varite, Inc - Short Hills, New Jersey (+1 location)

Job Description: Regulatory & Medical Affairs - Regulatory Studio - CMC Senior Manager Location: Hybrid (50% onsite) at either Lawrenceville in US or (US 100% Remote) PREREQUISITES BS/BA degree

from: resume-library.com - 2 days ago

Meet - , NJ, United States

Degree: Medical Doctorate (M.D.), D.O., or non-US equivalent. Experience: Minimum of 2 years in medical affairs, clinical trials, or clinical practice in the pharmaceutical industry or academia, with 3

from: linkedin.com - 28 days ago