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Years Drug Safety/Pharmacovigilance experience. Contribute to qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Pharmacovigilance, Epidemiology, etc.
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Kyowa Kirin is a fast growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four areas of unmet need: oncology, nephrology, immunology and CNS/movement disorders.
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Manage Arrowhead's QMS for safety/Pharmacovigilance procedures. Assist with preparation for regulatory inspections including a compiling of material relating to safety/pharmacovigilance reports and activities.
$85Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law.
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Dive into the dynamic world of AI and Digital Technologies at Genmab The Role: As an Associate Digital Product Manager in IT & Digital, you will have a critical role in overseeing the product strategy, development/implementation and management of technology products in different focus areas in Global Drug Safety and Pharmacovigilance.
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The Director of Pharmacovigilance (DPV) leads and/or oversees safety and benefit-risk management for assigned product(s), management of potential safety issues, identification of signals and their evaluation, and other activities such as drafting responses to regulatory inquiries on product safety issues for assigned product(s.
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Reporting to the Executive Director of Development Quality Assurance, the Senior Director of Pharmacovigilance QA serves as a strategic partner managing quality and regulatory compliance related to Good Pharmacovigilance Practices (GVP) and other related activities performed by Drug Safety & Pharmacovigilance and Medical/Clinical Departments.
$200,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Thought Leader Liaison (TLL) is a field-based, role that works closely with national and regional oncology and dermatology healthcare providers (HCPs), CTCL Centers of Excellence, and patient advocacy groups, to gain insights into the CTCL market, identify speakers/consultants, and help establish Kyowa Kirin as a leader in the MF/SS market.
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You will be joining the Product Team in Global IT that supports our Pharmacovigilance business function. Furthermore, you have: · Experience with maintaining applications from the field of PV · Deep business process knowledge in either Quality, Regulatory or Pharmacovigilance.
$155,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The role supports regulatory compliance with pharmacovigilance regulations, safety signal detection/management, and contributes to the overall benefit-risk management of Exelixis products. The role collaborates closely with Drug Safety Operations staff (on medical aspects of ICSRs) and Clinical Development (medical ICSR discussion and follow-up, as well as safety surveillance.
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Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science) and demonstrated experience in Pharmacovigilance case processing. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
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MedDRA and other dictionaries used in pharmacovigilance. Masters degree and 6 years of safety/ pharmacovigilance related experience. Pharmacovigilance Scientist, Senior Manager. Doctorate degree and 2 years of safety/ pharmacovigilance related experience.
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Role Summary: The Senior Director, Drug Safety and Pharmacovigilance will play a key leadership role in characterizing the safety profiles of Dyne products and mitigating and communicating their risks throughout the product lifecycle (from First-In-Human to post-marketing.
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Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes. Controller's data protection officer can be contacted at usprivacyoffice@kyowakirin.com.
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Demonstrates familiarity with pharmacovigilance and epidemiology related literature. 12+ years of clinical drug development experience, including 8+ years of patient safety pharmacovigilance experience.
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Title: pharmacovigilance Company: Kyowa Kirin
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