Pharmaceutical Regulatory Affairs Jobs in Cranbury, NJ

Experic - Cranbury Township, NJ 08512, USA

of relevant regulatory affairs experience in the clinical and commercial manufacturing space. Minimum of 10 years of relevant Regulatory Affairs experience (regionally or globally), in early and late $120000 - $150000 per year

from: applicantpro.com - More than 30 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 - 9 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 - 11 days ago

Cynet Systems - Princeton, NJ

Job Type: Contract Job Description: Pay Range: $60hr - $65hr Requirements: 7+ years of experience as BA. Working knowledge of Pharmaceutical R&D Life Sciences. Specific knowledge of Global Regulatory Affairs Depends on Experience

from: Dice.com - 5 days ago

Mindlance - Bridgewater, NJ, United States

of relevant Regulatory Affairs experience (regionally and/or global), in early development.

from: linkedin.com - 2 days ago

Lupin Pharmaceuticals Inc. - Somerset, New Jersey

years’ experience in the pharmaceutical industry with 3‐5 of those years in regulatory affairs preferred Prior experience of participating in managing, designing and implementing REMS systems (highly

from: resume-library.com - 3 days ago

Ascendis Pharma - Princeton, NJ

with Compliance, Legal and Regulatory to ensure that all US Medical Affairs activities and services are fully compliant with Ascendis SOPs and US as well as global regulatory and compliance rules/law. Requirements

from: workable.com (+1 source) - More than 30 days ago

The Fountain Group LLC - Bridgewater, New Jersey

and strategy in collaboration with GRT (Global Regulatory Team) and is accountable for the communication of the key outcomes to senior management. Experience: • At least 8-10 years of relevant pharmaceutical

from: resume-library.com - 2 days ago

Mindlance - Bridgewater, New Jersey

years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global). EEO: “Mindlance is an Equal Opportunity

from: resume-library.com - 4 days ago

Randstad - bridgewater, new jersey (remote)

of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. Must have: - Leadership $89 - $91.11 per hour

from: randstadusa.com - 5 days ago