Safety Associate - Princeton

The Safety Data Associate will support regulatory safety operations by collecting, organizing and maintaining product safety data within Excel-based systems. · ...

The Safety Data Associate will support regulatory safety operations by collecting, organizing, and maintaining product safety data within Excel-based systems. This role will also be responsible for communicating with external suppliers to obtain required documentation and ensure ...

Toxicology Safety Associate responsible for AI Support projects , ISA database support projects , study report summaries . Strong communication skills required.Ai Support projects for AI Improvements · ISA database support projects · study report summaries · ...

The Worldwide Patient Safety group is responsible for ensuring the safety of our medicines: The Worldwide Patient Safety group is responsible for pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, cont ...

The Safety Associate will oversee vendor management of single case processing and Business critical activities. They will organize workload in order to prioritize urgent deliverables, execute accurate timelines, and process cases in a timely manner. The associate will also serve ...

A demonstrated ability to work within defined departmental standards. · Ability to organize information from rough reports into a standard format. · An understanding of the conventions and singularities of a specific therapeutic area is a plus. · ...

+Safety Associate required with 4 year life sciences or health related degree and experience in pharmacovigilance or clinical medicine/nursing/pharmacy environment. · +Post-marketing and/or investigational drug safety reporting experience. · Demonstrated research/writing/presenta ...

++The Associate Director will oversee and implement operations of Pharmacovigilance in North America.+ · Responsibilities include the following: · ,+Ensure audit preparedness and manage regulatory and internal inspections,Draft any corrective action/preventative action plans (CAP ...

The Associate Director Drug Safety will oversee Pharmacovigilance in North America. He/She will communicate relevant information internally and with other members of SUN and its affiliates. · The position leads teams based out of USA, Canada & liaise with pharmacovigilance teams ...

We are searching for an Associate Director Safety Analysis Scientist to provide scientific expertise in safety assessment of assigned assets at Johnson & Johnson Enterprise Innovation. · ...

Job summary · At Genmab we are dedicated to building extraordinary futures together by developing antibody products and groundbreaking KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create champion and maintain a gl ...

The Associate Director will oversee pharmacovigilance operations in North America, ensure compliance with regulatory requirements, and communicate relevant information internally and externally. · Ensure audit preparedness and manage regulatory inspectionsDraft corrective action ...

SystImmune is a leading and well-funded biopharmaceutical company that specializes in developing innovative cancer treatments. This job opportunity involves leading medical assessment and interpretation of safety data from multiple sources. The individual will collaborate with cr ...

SystImmune is a leading biopharmaceutical company developing innovative cancer treatments. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. · ...

Responsible for executing US Adverse Event and Pharmacovigilance activities as required by FDA Regulations. · ...

Responsible for executing US Adverse Event and Pharmacovigilance activities as required by FDA Regulations. · ...

We offer an opportunity for you to learn and grow while making significant contributions to the company's success.This individual is to lead medical assessment and interpretation of safety data from multiple sources, including clinical trials, and literature reports. · ...

Dice is the leading career destination for tech experts at every stage of their careers. Our client, Tandym Tech, is seeking the following. Apply via Dice today · A New Jersey-based biotech company is actively seeking a new Associate Director of Global Drug Safety & Pharmacovigil ...

· SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibo ...

This role seeks an experienced Pharmacovigilance Systems professional to support Oracle Argus Safety system management. · ...