- Amgen (Washington, DC)
- …+ Processes and regulations for pharmacovigilance and risk management + Drug development and lifecycle management + Safety data capture in clinical ... time for a career you can be proud of. ** Pharmacovigilance Scientist, Senior Manager ** **Live** **What you...and conventions + MedDRA and other dictionaries used in pharmacovigilance + Methods of qualitative and quantitative safety… more
- ThermoFisher Scientific (Cambridge, MA)
- …of experience in the pharmaceutical/biotech industry with at least 5years in pharmacovigilance / drug safety (experience with adverse event monitoring and ... teams within Development. + Progress understanding and education of safety requirements for pharmacovigilance and other relevant...and programs is a plus) + Knowledge of the drug development process, GXP quality and compliance requirements, In… more
- Kelly Services (Bridgewater, NJ)
- …reports generated from company sponsored clinical trials. * Analyze metrics for critical Drug Safety processes to ensure compliance with SOPs and regulatory ... or signals; ensure accuracy and timely submission. * Inform manager and GPRM of safety related issues... Information **Requirements:** * Two to five years of Pharmacovigilance experience * Clinical safety and … more
- Mitsubishi Chemical Group (Jersey City, NJ)
- … safety topics for products working closely with Drug Safety Global Safety Team (GST) Chair (Medical Director). The Manager , Drug Safety will ... author safety aggregate reports as needed. The Manager , Drug performs medical analyses for risk...+ Strong knowledge of global regulatory requirements related to pharmacovigilance and drug safety . +… more
- Actalent (Morris Plains, NJ)
- ** Pharmacovigilance Manager ** Description: + Medical review of ICSRs. + MedDRA coding + Expectedness assessment. + Causality Assessment and Company Comment. + ... + Preparation of yearly schedule of periodic reports. + Ensure that all pharmacovigilance documents are prepared in time and are quality controlled. + Overview of… more
- BeiGene (San Mateo, CA)
- … sections of global regulatory inquiries and periodic reports including Development Safety Update Reports (DSURs), Periodic Adverse Drug Experience Report ... medical field or biological science and 8+ years of experience as a Safety ( Pharmacovigilance ) Scientist. OR MD (or internationally recognized equivalent) plus… more
- BeiGene (Emeryville, CA)
- … sections of global regulatory inquiries and periodic reports including Development Safety Update Reports (DSURs), Periodic Adverse Drug Experience Report ... medical field or biological science and 6+ years of experience as a Safety ( Pharmacovigilance ) Scientist. OR MD (or internationally recognized equivalent) plus… more
- BeiGene (Springfield, IL)
- …safety monitoring activities and contributes and assists in pharmacovigilance activities including benefit/risk and regulatory activities and interactions. ... sections of global regulatory inquiries and periodic reports including Development Safety Update Reports (DSURs), Periodic Adverse Drug Experience Report… more
Related Job Searches:
Drug,
Drug Safety,
Drug Safety Pharmacovigilance,
Manager,
Manager Drug,
Pharmacovigilance,
Safety,
Safety Manager,
Safety Manager Drug,
Safety Pharmacovigilance