Drug Safety & Pharmacovigilance Jobs in New Jersey

1 to 10 of 21 vacancies

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Global PV Submissions Specialist  

Clinical Resource Network (CRN) - Princeton, NJ, United States

submission reconciliations with local safety managers. Assist the Global Pharmacovigilance team with various projects to enhance system performance. Required Qualifications: Bachelor of Science or related

from: linkedin.com - 3 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 - 4 days ago

Associate Digital Product Manager, Global Drug Safety and Pharmacovigilance  

Genmab - Princeton, New Jersey

, determined to be our best, and authentic is essential to fulfilling our purpose. Associate Digital Product Manager, Global Drug Safety and Pharmacovigilance This person will be based out of Princeton, NJ

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from: resume-library.com - 4 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 - 4 days ago

Senior Pharmacovigilance Associate  

Tandym Group - Florham Park, NJ, United States

, compiling data for FDA aggregate report submission Author or review FDA aggregate safety reports such as periodic adverse drug experience reports (PADERs) along with the cover letter Research and draft

from: linkedin.com - 4 days ago

Senior Business Analyst  

Katalyst Healthcares & Life Sciences - South Plainfield, New Jersey

, and ensuring that our pharmacovigilance activities align with regulatory requirements and industry best practices. The ideal candidate will have a strong background in drug safety and pharmacovigilance, combined

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from: resume-library.com - 3 days ago

GPV Case Management Product Specialist  

GForce Life Sciences - Princeton, NJ, United States

ICSR processing Coordinate internally and with external pharmacovigilance providers (CROs) and Business Partners on Drug Safety and Pharmacovigilance case management issues Support PV management

from: linkedin.com - 17 days ago

Sr Manager, Drug Safety Data  

Mitsubishi Tanabe Pharma - Jersey City, New Jersey

requirement(s), identifies drug safety data quality rules, and design and program reports based on the data reporting requirement in accordance with SOPs, client requirements, and regulatory guidelines

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from: resume-library.com - 3 days ago

Director Clinical Safety  

HireTalent - Basking Ridge, New Jersey

of the NDA, CSR, and IB 3-5 years of Pharmacovigilance (PV)/drug safety experience in pharmaceutical drugs either from relevant work experience within the industry or related healthcare work Demonstrated

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from: resume-library.com - 10 days ago

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Associate Director, Drug Safety  

Sun Pharma - Princeton, New Jersey, USA

The Associate Director/ Director, Drug Safety (Title is comensurate with experience) will oversee and implement operations of Pharmacovigilance in North America and communicate relevant information

from: Ivyexec.com - 5 days ago


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