Regulatory Jobs in Czech Republic

Job DescriptionThe PositionWe are looking for Veeva Vault RIM (Regulatory Information Management) expert to lead the configuration development and optimization of our Veeva RIM platform to support pharmaceutical and biological Development. This role will lead the further technical implementation of...

Job DescriptionWe are looking for one motivated and talented individual to join our company as a Regulatory Affairs Senior Specialist in Prague.The role reports to the International Labeling Support (ILS) Associate Director and will partner cross-functionally within GRACS and across divisions to sup...

Job DescriptionWe are looking for one motivated and talented individual to join our company as a Regulatory Affairs Senior Specialist in Prague.The role reports to the International Labeling Support (ILS) Associate Director and will partner cross-functionally within GRACS and across divisions to sup...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Es...

The Senior Specialist Regulatory and PV Network is responsible for developing the strategy based on regulatory requirements and for driving regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other functional areas includ...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

The Specialist Regulatory and PV Network is responsible for providing the strategy based on regulatory requirements and for completing regulatory and PV deliverables based on an established PV and regulatory plan. They also serve as a liaison between regulatory and other functional areas including e...

Join our international team and support regulatory aspects of clinical research projects streamlining communication maintaining electronic systems and managing documents.Hybrid working arrangement in Prague the Czech RepublicYou will:Be the point of contact for clinical project teams and support ser...

Join our team of experts in regulatory submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products while taking a step further in your professional career.Hybrid working arrangement in Prague the Czech RepublicYour role:Prepare and overs...