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Drug Safety Jobs in New Jersey

1 - 15 of 21
1 - 15 of 21
Search Results - Drug Safety Jobs in New Jersey
Cost Management Incentives Inc-Jersey City
Title: Sr. Drug Safety Specialist / Safety Manager (Temporary Contractor) Department: Drug Safety Supervisor: Associate Director, Project Management POSITION OVERVIEW/SUMMARY Job Description: The Senior Drug Safety Specialist / Safety...
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Daiichi Sankyo, Inc.-Trenton
Bachelors Degree Science degree required Masters Degree preferred or PharmD preferred or RN degree preferred Experience Qualifications 4 or More Years drug safety experience with technical experience in Electronic Data Capture and Safety Reporting...
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LanceSoft Inc-Madison (NJ)
Masters) Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with 5+ years of development experience. 5+ years of experience with Databases (Postgres, Oracle, MS Access, Impala, SharePoint List etc.) 5+ years Drug Safety...
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1 similar job: Lawrenceville
Pyramid Consulting, Inc-Titusville (NJ)
other responsibilities as deemed appropriate for coordinator role to support compliance to pharmacovigilance requirements. Key Requirements and Technology Experience:  •  Key Skills: ticketing system(s) ,Adverse reporting experience ,Drug safety (Must...
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Artech LLC-Madison (NJ)
to facilitate decision-making process  •  Assess and interpret the process impact of new PV tools and processes Skills/Knowledge Required:  •  Life Sciences, Information, or similar background (Bachelors, Masters)  •  5+ years Drug Safety/Pharmacovigilance...
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Daiichi Sankyo, Inc.-Jersey City
A minimum of 5 years of professional management experience in PV required  •  10+ years of Drug Safety/Pharmacovigilance experience, including both investigational and marketed products required  •  Knowledge of Adverse Event and drug coding conventions (MedDRA...
Artech LLC-Madison (NJ)
or similar background (Bachelors, Masters)  •  5+ years Drug Safety/Pharmacovigilance experience  •  Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with 5+ years of development experience  •  Databases (Postgres, Oracle, MS Access, Impala...
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Daiichi Sankyo, Inc.-Newark
A minimum of 5 years of professional management experience in PV required  •  10+ years of Drug Safety/Pharmacovigilance experience, including both investigational and marketed products required  •  Knowledge of Adverse Event and drug coding conventions (MedDRA...
Daiichi Sankyo, Inc.-Trenton
A minimum of 5 years of professional management experience in PV required  •  10+ years of Drug Safety/Pharmacovigilance experience, including both investigational and marketed products required  •  Knowledge of Adverse Event and drug coding conventions...
mindmatch.ai -
Daiichi Sankyo, Inc.-Trenton
A minimum of 5 years of professional management experience in PV required  •  10+ years of Drug Safety/Pharmacovigilance experience, including both investigational and marketed products required  •  Knowledge of Adverse Event and drug coding conventions (MedDRA...
Princeton (NJ)
candidate nomination through registration and lifecycle management. The Dev DMPK team is responsible for characterizing the ADME properties, and drug-interaction potential of drug candidates. Working closely with drug safety"and clinical pharmacology, Dev...
pharmiweb.jobs -
Integrated Resources, Inc-Lawrenceville (NJ)
Life Sciences, Information, or similar background (Bachelors, Masters) " 5+ years Drug Safety/Pharmacovigilance experience " Advanced Tableau, Spotfire, Power BI, SAP Business Objects (BO) skills with 5+ years of development experience " Databases...
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Daiichi Sankyo, Inc.-Trenton
Drug Safety Update Reports (DSURs), and other safety-related documents, in collaboration with the Safety Physician Maintain up-to-date knowledge of all-important advances within a disease area through scientific literature, critical meetings...
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Daiichi Sankyo, Inc.-Newark
accountable for safety surveillance and risk management activities for his/her portfolio. Serves as the company's senior representative with key high-level internal and external stakeholders on important drug safety issues supporting Global Medical Safety Lead...
Daiichi Sankyo, Inc.-Trenton
on compound/disease and dose modifications/discontinuations as well as management of adverse events based upon approved Safety Management Team (SMT) materials  •  Supports overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug...
mindmatch.ai -
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