Pharmaceutical Risk Management Jobs in Princeton, NJ

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Manager, R&D Quality Risk Management  

Planet Pharma - Princeton, NJ, United States

job experience may be considered. Minimum of 6 years R&D focused pharmaceutical/Health Care experience in a GCP regulated environment including some experience in R&D Quality Risk Management or R&D Quality

from: linkedin.com - 13 days ago

Clinical Quality and Compliance Specialist (GCP)  

Russell Tobin - Princeton, NJ, United States

+ years R&D focused pharmaceutical experience in a GCP regulated environment Experience in R&D Quality Risk Management or R&D QA systems and Health Authority regulations Experience with drug development

from: linkedin.com - 17 days ago

Quality Manager  

Katalyst Healthcares & Life Sciences - Princeton, New Jersey

. Requires excellent verbal/written communication, negotiation/influencing, leadership and risk assessment skills. Experience in negotiation/influencing and management of remote third party partners Requires

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from: resume-library.com - 5 days ago

Associate Director, PV Sciences  

Taiho Oncology - Princeton, NJ

, * Proficiency in signal detection, safety surveillance, risk mitigation and risk management. * Experience directly managing people and/or leading a cross-functional team is a plus. * Expertise in relevant food

from: Taiho Oncology - 9 days ago

Sr. Consultant, Clinical Trials  

Endeavor Consulting Group - Princeton, New Jersey

Minimum 4 years of experience in clinical trial management, preferably in the pharmaceutical industry In-depth knowledge of international regulatory requirements and guidelines for clinical research Strong

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from: resume-library.com - 11 days ago

Senior Analyst, Government Rebate Operations (GRO) Contracts  

Johnson & Johnson - Raritan, NJ

), State Pharmaceutical Assistance Programs (SPAPs), and AIDS Drug Assistance Programs (ADAPs). The Sr. Analyst will support the efficient and compliant management of GRO contracts including, but not limited USD 76,000.00 - 121,900.00 per year

from: Dice.com - 28 days ago

Sr Director Quality Assurance Operations  

Insmed Incorporated - Bridgewater, New Jersey

and Risk Management experience preferred, i.e. ISO 13485 and ISO 14971. Demonstrate ability to manage projects and variable workloads. Excellent communication and coaching skills (verbal and written). Highly

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from: resume-library.com - 7 days ago

Engineer, Device Technology  

Merck - Rahway, NJ 07065

and written communications Preferred Three plus years in medical device, pharmaceutical or in biotech organizations Three plus years in design control, risk analysis and change control management for medical

from: Pharmadiversityjobboard.com - 8 days ago

Associate Director, Clinical Supply Integrator  

Johnson and Johnson - Horsham, PA

, while proactively managing risk to avoid patient impact. Key Responsibilities: * Study drug management for pharmaceutical R&D clinical trials. * Ensure 99.5% successful dose, optimized inventory levels

from: Johnson and Johnson - 7 days ago

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Director, Medical Safety Officer, Oncology  

Johnson & Johnson - Horsham, PA

/risk, when appropriate, to the Sr. Director Product Safety Head, the VP Therapeutic Area Safety Head (TASH), the Head of Global Safety Strategy & Risk Management (GSSRM), the Chief Safety Officer (CSO USD 186,000.00 - 322,000.00 per year

from: Dice.com (+1 source) - 15 days ago


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