Drug Safety & Pharmacovigilance Jobs in Berkeley Heights, NJ

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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 - 14 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 - 13 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 - 14 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 - 14 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 - 13 days ago

Executive Director DSPV Medical Safety  

Insmed Incorporated - Bridgewater, New Jersey

and champions issue resolution. Oversee medical safety and pharmacovigilance activities conducted in partnership with external business partners or outsource to vendors and contract research organizations (CROs

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from: resume-library.com - 6 days ago

Associate Director/Director, Global Safety Lead - Remote  

Agios Pharmaceuticals - Anywhere, New York, USA

experience in drug safety pre-approval (ranging from early to late-stage) and/or in the post-marketing setting Demonstrated knowledge of pharmacovigilance and risk management Solid knowledge and understanding

from: Ivyexec.com - 7 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 - 20 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 - 22 days ago

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Director, Medical Affairs (Rare Diseases)  

Florham Park, NJ

in collaboration with project teams; collaborate with the drug safety team members to optimize pharmacovigilance activities, including evaluation of reports of spontaneous and clinical adverse events and monitoring

from: Pharmadiversityjobboard.com - 27 days ago


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