Drug Safety & Pharmacovigilance Jobs in Somerset, NJ

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Safety Case Management Product 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 - 5 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 - 7 days ago

Sr. Director, PV Medical Surveillance  

Taiho Oncology - Princeton, NJ

/benefit profile for responsible compounds, as well as regulatory guidelines as they pertain to drug safety/pharmacovigilance. * Responsible for Individual Case Safety Report (ICSR) review. Ensures

from: Taiho Oncology - 2 days ago

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 - 12 days ago

GPV Case Management Product Specialist  

GForce Life Sciences - Trenton, 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 - 6 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

Sr. Director, Global Drug Safety  

Adecco - Elizabeth, NJ, United States

) Strong understanding of pharmacovigilance regulatory requirements Knowledge of drug development, safety monitoring and risk/benefit analysis Experience with individual case medical review, signal detection

from: linkedin.com - 15 days ago


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