Drug Safety & Pharmacovigilance Jobs in Elizabeth, NJ

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GPV Case Management Product Specialist  

GForce Life Sciences - Princeton, NJ, United States

in the oversight of vendor-supported ICSR processing Coordinate internally and with external pharmacovigilance providers (CROs) and Business Partners on Drug Safety and Pharmacovigilance case management issues

from: linkedin.com - 7 days ago

Clinical Quality and Compliance Specialist (GCP)  

Russell Tobin - Princeton, NJ, United States

! Responsibilities Manage assigned R&D Quality Risk Management activities – assessment of QC of clinical trials execution in a GCP regulated environment Support Drug Safety Pharmacovigilance, Computer System

from: linkedin.com - 10 days ago

Clinical Safety & Risk Management Physician  

Merck - Rahway, NJ 07065

Job Description Our Clinical and Pharmacovigilance Teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications

from: Pharmadiversityjobboard.com - 11 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 - 27 days ago

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 - 26 days ago

Clinical - Pharmacovigilance (PV) Scientist  

TechDigital Corporation - Madison, New Jersey

pharmacovigilance regulatory compliance with oversight, as needed. Position Responsibilities • Lead Safety Data Review (SDR) Teams and participate in related PV and product-development subteam(s). Appropriately

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from: resume-library.com - 6 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 - 27 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 - 4 days ago

Pharmacovigilance Associate  

Florham Park, NJ

Insight Global is looking for a Pharmacovigilance Associate for one of our clients to sit in Florham Park, NJ. They focus within women's health drug products specifically and have increased workload

from: Pharmadiversityjobboard.com - 13 days ago

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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 - 26 days ago


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