Clinical Research Regulatory Specialist
We have 67 ads for keyword clinical research regulatory specialist
(0.001 seconds)Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
IPM Specialist
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Full-timeJob Family: Legal, Compliance & AuditSub Job Family: Intellectual Property ManagementPreferred type of working: On-PremiseYears of Experience: 12
Manufacturing Specialist CAR-T
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Full-timeJob Family: ManufacturingSub Job Family: Production - Biosimilar (Drug Product)Business unit: BiologicsYears of Experience: 6 - 12 Job DescriptionDr
MSAT Associate : Upstream
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Full-timeJob Family: Research & DevelopmentSub Job Family: Upstream R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 6 -
MSAT Specialist - Downstream
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Full-timeJob Family: Research & DevelopmentSub Job Family: Downstream R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 6 -
IPM Specialist
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Full-timeJob Family: Legal, Compliance & AuditSub Job Family: Intellectual Property ManagementPreferred type of working: On-PremiseYears of Experience: 12
Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Associate Regulatory Specialist
Work Mode : Hybrid Location: Gurugram Summary: As an individual contributor, the function of the Associate Regulatory Affairs Specialist is to support the
Medical Information Specialist
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Full-timeDepartment: Customer ServiceJob Family: Medical & Regulatory Affairs Company DescriptionAt EVERSANA, we are proud to be certified as a Great Place
IPM Specialist
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Full-timeJob Family: Legal, Compliance & AuditSub Job Family: Intellectual Property ManagementPreferred type of working: On-PremiseYears of Experience: 10
MSAT Specialist - Downstream
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Full-timeJob Family: Research & DevelopmentSub Job Family: Downstream R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 7 -
MSAT Associate : Upstream
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Full-timeJob Family: Research & DevelopmentSub Job Family: Upstream R&D - BiosimilarPreferred type of working: On-PremiseYears of Experience: 7 -
Program Marketing Specialist
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Full-timeShift: DayTravel Requirements: 50% of the timeEmployee Type: EmployeeGlobal Job Level (HCM): Professional 3 (9) Company DescriptionAt Intuitive, we
IPM Specialist
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Full-timeJob Family: Legal, Compliance & AuditSub Job Family: Intellectual Property ManagementPreferred type of working: On-PremiseYears of Experience: 10
Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Associate Regulatory Specialist
Work Mode : Hybrid Location: Gurugram Summary: As an individual contributor, the function of the Associate Regulatory Affairs Specialist is to support the
Regulatory Affairs Specialist | (A-052)
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to
Study Startup Lead
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Full-time Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A
Safety Specialist | [ZUL-817]
Job Description Performs day-to-day Pharmacovigilance (PV) activities performed within a highly regulated environment and driven by strict timelines.
Lead Auditor, Specialist
Department : Quality Audits GBS Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way?