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Financial Supply Chain Specialist
Job Title Supply Chain Associate Specialist Location: County Cork, Ireland Company Statement My client is a Global Pharmaceutical company tha...
New
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EU Regulatory Affairs
Brief Description:The primary responsibility is the creation of regulatory documents and development of regulatory strategy to achieve regulatory appr
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Patient Services Coordinator II
Brief Description: Provide consistentcustomer service support to all stakeholders for the assigned program(s) Requirements: • High School Graduate; so
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Regulatory Affairs Intern (12 months)
Who we areRoche is the world's leading research-based healthcare company, providing innovative products to both the Pharmaceutical and Diagnostics ind
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Safety Writer
This is a great opportunity for experienced Safety Writers working within the pharmaceutical, biotech and Contract Research Organisation (CRO) sector,
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Communications Lead, Operational Excellence
Title: Communications Lead, Operational Excellence, Novartis, Dublin, IrelandWhy Novartis817 million. That's how many lives our products touched in 20
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Business Planning Analyst / Finance Analyst - Novartis!
Business Planning Analyst / Commercial Analyst Manager, Novartis, Dublin, Ireland** Business Analyst / Commercial Analyst / Finance Analyst / Analysis
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Senior Clinical Research Associate (6 months contract) IDF/France
Job SummaryCome and work for a sought-after industry leader!Roles & Responsibilities of the positionMission :Vos responsabilités seront les suivantes
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Planning Analyst - P
Description: Job title: Planning Analyst Location: South of GermanyDuration: PermanentTalentSource Life Sciences, the division of CROMSOURCE dedicated
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Contract Management Specialist
The Contract Management Specialist is responsible for the timely and appropriate execution of Confidentiality Disclosure Agreements (CDAs), Clinical
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Clinical Trial Assistant
Clinical Trial Assistant (CTA) - Permanent - Boston, MADo you want to be part of an award-winning global clinical research organisation who is positiv
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Clinical Research Associate
Clinical Research Associate - South West England (Home Based)Clintec is actively recruiting for a Clinical Research Associate to join our expanding gl
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Regulatory Project Manager - Registrations & Post marketing / National/MRP/DCP/CP / Middlesex
Regulatory Project Manager. EU Regulatory scope. Specialist Pharma.
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Principal Regulatory Executive / CMC Variations / Drug Development / Lead Project Teams / Middlesex
Principal Regulatory Executive. EU focus. Registrations & Post marketing; PM and small team to supervise.
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Regulatory Affairs Director / Essex / Consultancy, Strategy and 'Hands-on' - Lead the Team
Regulatory Affairs Director; Consultancy; Team Management; Strategy, Tactics and Clinical Development; Biologic Product experience; Essex
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Regulatory Affairs Director / Advanced Therapies / Lead a Team / Development & Strategy
Director Regulatory Affairs, Advanced Therapies. Team Leadership; Strategy and Clinical/Development; Consultancy; Essex
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Regulatory Affairs Manager Europe & ROW / Emerging Markets / International - based Ireland
Regulatory Affairs Manager – Europe and International/ROW/Emerging Markets. Registrations & Post Marketing; Based Cork, Ireland
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Medical Monitor, UK
The Medical Monitor (MM) is responsible for the development, execution and subsequent interpretation of data for GMAF (Global Medical Affairs).
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Associate Director of Regulatory Affairs, Europe
Linical Co. , Ltd. (‘Linical’) is a premier global CRO headquartered in Osaka, Japan, listed in the prime segment of the Tokyo Stock exchange, and ...
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Biostatistical SAS Programmer
Linical Co. , Ltd. (‘Linical’) is a premier global CRO headquartered in Osaka, Japan, listed in the prime segment of the Tokyo Stock exchange, and ...