Drug Safety

Location: Barcelona (on-site) Do you have expertise in, and passion for clinical development?Are you looking to work at the cutting-edge, where scientific

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports,

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports,

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports,

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports,

Responsible for the drug surveillance program including the necessary follow-up, risk assessment, and relatedness to product on adverse reaction reports,

When our values align, there's no limit to what we can achieve.If you want to be part of a leading CRO and transform scientific discoveries into new

Work Schedule Other Environmental Conditions Office Job Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact

Medical Director, Early Global Development, Oncology R&DDo you have expertise in, and passion for clinical development? Are you looking to work at the

Work Schedule OtherEnvironmental Conditions OfficeJob Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on

When our values align, there's no limit to what we can achieve.If you want to be part of a leading CRO and transform scientific discoveries into new

SummaryMonitors and audits the company's drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on

SummaryMonitors and audits the company's drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on

SummaryMonitors and audits the company's drug, biologics or medical devices surveillance program including the intake, evaluation, processing and follow-up on

Precision Medicinewithin AstraZeneca focuses on matching medicines to those patients who will benefit from them most and delivers companion or complementary

Director Scientist, Early Global DevelopmentThe Director Scientist is an important part of the Project Team, working synergistically with program and study

Help Help Duties Program Management (includes but not limited to): 65% Plans, organizes, develops, implements, and manages a diverse and comprehensive fitness,

Job ID: REQ-10011542Aug 29, 2024SpainSummary: Monitors and audits the company's drug, biologics, or medical devices surveillance program including the intake,

Detalles del empleo Así es cómo la información del empleo se alinea con tu perfil.Tipo de empleo - Jornada completa Ubicación Madrid, Madrid provincia

This is what you will do : The Associate Director of Global Medical Information and Medical Review is responsible for managing Global Medical Information