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We want to make getting prescriptions easy. We untangle the prescription process for pharmaceutical manufacturers and create a clear path allowing patients to build trusting relationships with their medication brands. · ...
Hanover Township $18.96 - $28.80 (USD) Full time3 weeks ago
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· Overview · Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus ...
Somerset, New Jersey, United States $90,000 - $150,000 (USD) per year5 days ago
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Review and approve adverse event reports for pharmaceutical products. · ...
Madison1 month ago
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c08 - medical and regulatory affairs / pharmacovig - pharmacovigilance specialist
Only for registered members
The Pharmacovigilance (PV) Analytics and Reporting Specialist, PV Analytics Center of Excellence is responsible for successful execution, · and close-out of activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. ...
Madison1 month ago
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We are hiring Clinical Information Specialist - II (Associate) for one of our clients. · This position will be responsible for tracking, disposition and maintenance of archival information for database requests and will include updating reportability rule and product configuratio ...
Rahway1 month ago
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We are seeking a Document Management Specialist to join our team in Summit, NJ. The successful candidate will be responsible for uploading documents into SharePoint system for efficient record keeping and back-up as SharePoint administrator for Global Risk Management. · Upload do ...
Summit1 month ago
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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 ...
Summit1 month ago
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The Specialist for Complaints at the S-12 Cell Therapy Manufacturing is responsible for the process and system ownership of the Product Quality Complaint (PQC) quality system module.This role has a high impact on departmental performance and broad quality initiatives requiring bo ...
Summit1 month ago
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· About Tonix* · Tonix is a fully integrated biotechnology company, publicly traded on NASDAQ (ticker: TNXP), with marketed products and a pipeline of development candidates The Company is focused on commercializing, developing, discovering, and licensing therapeutics to treat a ...
Berkeley Heights, NJ1 week ago
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We are seeking a high-impact Subject Matter Expert with expertise in Pharmacovigilance and Safety Systems to give the solutions.The ideal candidate will be an expert in Pharmacovigilance business processes and Safety Systems configuration, with extensive experience in global PV r ...
New York3 weeks ago
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We are seeking a high-impact Subject Matter Expert with expertise in Pharmacovigilance and Safety Systems to give the solutions.The ideal candidate will be an expert in Pharmacovigilance business processes and Safety Systems configuration, with extensive experience in global PV r ...
New York1 month ago
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Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward. · R&D Partners is seeking a Senior Pharmacovigilance Manager to lead and manage key projects within the pharmacovigilance sector. · Lead and manage projects ...
Basking Ridge3 weeks ago
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+Job summary · SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ.++Bachelor's degree in life sciences, pharmacy, nursing, or related field · 3-5+ years of experience in pharmacovigilance case processing prefe ...
Princeton $85,000 - $115,000 (USD)1 month ago
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Lupin is comprised of a fast growing, innovative and robust team of manufacturing, Research and Development and commercial divisions. Together these entities make up the generic and branded U.S. business. Lupin has a significant generic pipeline, and a branded focus on women's he ...
Somerset $90,000 - $150,000 (USD)4 days ago
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Excellent opportunity for a customer service specialist with experience in business to business customer service. · This is a contract role with potential to convert to a permanent position. · Work with a global organization that values work/life balance. This is a hybrid role th ...
Warren Township1 month ago
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We are seeking a high-impact Subject Matter Expert with expertise in Pharmacovigilance and Safety Systems to give the solutions. · Expertise in PV Business Processes and Safety Systems Configuration: Combine deep knowledge of Pharmacovigilance business processes with hands-on exp ...
New York City Metropolitan Area1 month ago
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At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, cel ...
Bridgewater Township $42 - $53 (USD)1 week ago
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Join a leading pharmaceutical company to help keep life-changing science moving forward. · Lead and manage projects by setting goals, creating timelines, and ensuring deliverables are met. · Collaborate with teams to identify and address risks, issues, and dependencies. · ...
Basking Ridge, NJ3 weeks ago
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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. · ...
Princeton $250,000 - $275,000 (USD) Full time1 month ago
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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. · ...
Princeton $250,000 - $275,000 (USD)1 month ago
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Work with team of medical information professionals to manage department workflow of unsolicited medical inquiries. · Recognize and forward adverse drug events. · Research and respond to requests for scientific/medical information using various search techniques. · ...
Madison1 month ago
Principal Pharmacovigilance Specialist - Rahway - beBeePharmacovigilance
Job title: Clinical Safety and Risk Management Associate Principal Scientist
Description
Job Title:
Clinical Safety and Risk Management Associate Principal Scientist
Key Responsibilities:
The Clinical Safety and Risk Management Medical Associate Principal Scientist performs primary medical review of serious adverse experience (AE) reports to monitor the safety profile of assigned products. This involves assessing causality, analyzing aggregate data, and authoring safety documents in collaboration with other teams.Primary activities include:
Key tasks also involve working closely with cross-functional teams to develop strategies that ensure compliance with regulatory requirements while maintaining accurate product communications.
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c08 - medical and regulatory affairs / pharmacovig - pharmacovigilance specialist
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