Clinical Trials Jobs in Czech Republic

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Essential FunctionsOversee the execution of Site Activat...

Job Description SummaryThe SSO Site Partnership Manager optimizes the cooperation with selected trial sites considered key accounts for Novartis with huge potential to significantly contribute to the portfolio execution aiming to improve performance in clinical studies regarding patient numbers time...

Work ScheduleOtherEnvironmental ConditionsOfficeJob DescriptionConducts all clinical trials (studies) according to ICH GCP local regulations study protocol and company processes. Ensures the medical wellbeing and safety of the participants through the safe performance and execution of the studies. M...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specifi...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Sr Clinical Trial Manager/Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from eva...

Work ScheduleOtherEnvironmental ConditionsOffice Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Will work with hazardous/toxic materialsJob DescriptionConducts multiple ongoing clinical trials of varying size and complexity involvi...

For the Client:To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an...

For the Client:To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an...

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...

Clinical Trial AdministratorResearch & DevelopmentCzech RepublicReady to help deliver clinical trials that bring life-changing treatments to patients Your precision and dedication can turn scientific breakthroughs into real-world impactso patients benefit sooner.Your new roleAs a Clinical Trial Adm...

Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Global Regulatory Affairs and Clinical Safety (GRACS) organization in the EUEEMEA Regulatory Operations (RRO-EUEEMEA) Team.The RDP is responsible for publishing key regulatory submissions in the region and supporting the publis...

Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Global Regulatory Affairs and Clinical Safety (GRACS) organization in the EUEEMEA Regulatory Operations (RRO-EUEEMEA) Team.The RDP is responsible for publishing key regulatory submissions in the region and supporting the publis...

Job DescriptionThe Regulatory Affairs Operations will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and supporting business pro...

Job DescriptionThe Regulatory Affairs - System Process & Innovation will support regional activities associated with the implementation and support of Global Regulatory Affairs Compliance and Safety (GRACS) Digital Strategy projects and systems. With some understanding of regulatory affairs and sup...

Job DescriptionThe Senior Specialist of Digital Innovation & Systems will be accountable for the oversight of various tools and systems utilized by the Regulatory Planning and Publishing (RPP) Team. This position will understand the enterprise-wide tools utilized by RPP and the implications of the G...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

At AstraZeneca we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial thinking big and working together to make the impossible a reality. If you are swift to action confident to lead willing to collaborate and curious about what science can do...

At AstraZeneca we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial thinking big and working together to make the impossible a reality. If you are swift to action confident to lead willing to collaborate and curious about what science can do...

The Medical Director CZSK will lead the affiliate medical department set and execute Medical Affairs strategies for the affiliate medical department and ensure the affiliate medical team contributes valuable strategic input to Global Medical Affairs (GMA) Therapeutic Area strategic medical affairs p...

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to large generic post-marke...