Vice President, Global Drug Safety - New Providence, NJ

Ensuring that individual Adverse Event Case Reports are evaluated, investigated and accurately computerized. · Receipt · Execute receipt of Drug Safety phone calls and complete telephone AE form Create phone call communication logs in ARISg Triage · Support the triage of cases co ...

Position is for Sr. Documentation Specialist. · Support the Global Patient Safety & Epidemiology (GPSE) team in reviewing files for potential source documentation. · ...

We are seeking a dynamic, focused and creative individual to join our growing team. This role will be responsible for several portions of the adverse event case processing workflow including receipt, evaluation, registration, partial data entry, documentation and reporting of adv ...

The position is responsible for managing aggregate safety reports (ASRs) for development and marketed products. · Manage project schedulesTrack receipt of contributions for ASRsCreate and manage workflows for each of the ASRs in the document management system · ...

+Job summary+Transforming Cancer Therapy Together · At ADC Therapeutics, we are passionate about revolutionizing cancer treatment.When you join our team, you become part of a mission-driven group of talented individuals dedicated to making a difference in patients' lives. · +Qual ...

This position will be accountable for all of the activities and deliverables of the Drug Safety function including providing operational and medical oversight of safety activities for all ADC Therapeutics medicinal products administered to humans and ensuring regulatory requireme ...

This is a job opportunity for a Drug Safety Vice President at ADC Therapeutics. · ...

The Pharmacovigilance Operations Manager plays a critical role in ensuring patient safety and operational excellence across Acadia's global clinical development programs. · ...

Integrated Resources Inc is a premier staffing firm recognized for excellent service and integrity. · Monitor and manage dedicated DSU mailboxes · Maintain local documentation as required by legislation · ...

The Director Drug Safety Physician is responsible for leading the Global Safety Team(s) to develop safety strategies ensure patient safety regulatory compliance products in development marketed. · ...

++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 ...

Performs medical assessment and related activities for single cases. · ...

The Director Drug Safety Physician is responsible for leading Global Safety Teams to develop safety strategies ensure patient safety regulatory compliance products development marketed. · Ensure high quality accurate timely medical contributions safety evaluation Kyowa Kirin prod ...

The Director Drug Safety Physician is responsible for leading Global Safety Teams in developing safety strategies ensuring patient safety and regulatory compliance for products in development and/or marketed. · ...

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 ...

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 ...

The Director, Drug Safety Physician is the Lead of the Global Safety Team(s) to develop safety strategies to ensure patient safety and regulatory compliance for products that are in development and / or marketed. · ...

This is a Drug Safety Data Management Specialist role that requires entering applicable information into the global safety database for initial or follow up cases received via paper, fax or email. · ...

This is a safety data management specialist role that involves reviewing and preparing reports of adverse drug experiences to determine the safety profile of Pfizer's products. · It requires liaising with key partners and stakeholders regarding safety data collection and reconcil ...

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 ...