Pharmaceutical Regulatory Affairs Jobs in Trenton, NJ

1 to 10 of 11 vacancies

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Safety Case Management Product Specialist  

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

GPV Submission Specialist  

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

Pharma Business Analyst with Regulatory Experience  

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 - 2 days ago

Head of US Medical - Endocrine Medical Affairs- Job ID: 1323  

Ascendis Pharma - Princeton, New Jersey

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

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from: resume-library.com (+1 source) - 10 days ago

Manager Global CMC Regulatory Affairs  

Johnson and Johnson - Raritan, NJ

Affairs * Conducts due diligence/licensing evaluations where needed * Bachelors in Science (engineering, biological, pharmaceutical or chemical) with minimal 6 years of proven experience or equivalent

from: Johnson and Johnson - 6 days ago

Medical Director- Neurology  

Spark Therapeutics - Philadelphia, PA, US

and/or clinical experience; global experience preferred; Prior pharmaceutical experience in neurology (Clinical Development or Medical Affairs), and prior experience in conducting clinical research preferred; gene

from: Spark Therapeutics - 20 days ago

Sr. Regulatory Operations Specialist  

Zachary Piper Solutions, LLC - Philadelphia, PA

for external vendor communication. Technical Requirements for the Sr. Regulatory Operations Specialist Bachelor's degree required, with over three years of pharmaceutical/biotech industry experience, including USD 45.00 - 50.00 per hour

from: Dice.com - 12 days ago

Consultant Regulatory Affairs Associate  

Lupin Pharmaceuticals Inc. - Somerset, New Jersey

in the pharmaceutical industry with 1-2 of those years in regulatory affairs preferred Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment

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from: resume-library.com - 12 days ago

Regulatory Affairs Specialist, Cell & Gene Therapy  

Zachary Piper Solutions, LLC - Philadelphia, PA

, including trackers, SharePoint sites, and file sharing tools. Qualifications of the Regulatory Affairs Specialist, Cell & Gene Therapy 3+ years of pharmaceutical/biotech industry experience, with 2+ years USD 40.00 - 55.00 per hour

from: Dice.com - 14 days ago

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Senior Director, Global Regulatory Leader, CAR-T Therapy  

Johnson and Johnson - Raritan, NJ

years in drug development any of the following areas (e.g. Global Regulatory Affairs, R&D or health authority role) is required. * 10 years within the pharmaceutical/biotech industry is required, along

from: Johnson and Johnson - 13 days ago


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