Clinical Research Jobs in Prague

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and Functional Service (FSP) solutions.J...

PSI is seeking a Medical Monitor (Oncology) to join our international Medical Monitoring team.In this role you will provide medical oversight and expertise across global clinical trials working closely with study sponsors investigators sites project teams and other clinical research professionals. Y...

The Project Manager is responsible for the planning management and control projects run by the IT team in the delivery of technology to the Ergomed business and the delivery and hand over of the systems and capabilities into the production systems and business environments within defined and agreed...

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

The Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholdersAccou...

Providing support to other activities undertaken by the project team on behalf of the client and the companyLine Manages assigned ICSR staffCreates and maintains project specific KPIs for contracted ICSR activities (this includes optimizing procedures trainings and any other actions to increase ICSR...

The Director Business and Process Optimization serves as a key member of the leadership team providing strategic leadership in the direction and execution of the operations and resourcing for the department in a complex cross-functional environment to develop and execute strategies that ensure conti...

In this role you will be responsible for managing and optimizing COA/eCOA systems for clinical trials. Your expertise will be vital in ensuring their smooth integration and effective implementation which will be key to the success of our projects.Full-time employment based in CzechiaYou will:Support...

Responsible to coordinate and develop competitive and flexible strategies for potential awards in oncology and oncology-related indications leveraging expertise operational capabilities and technologies to ensure client needs are addressed in the pre-award activities.Serves as the lead oncology stra...

Collects validates and maintains data from internal and external sources to support feasibility and operational activities.Analyses clinical trial site investigator and operational data to identify trends patterns and opportunities for improvement.Develops and maintains standard reports dashboards a...

Job DescriptionAs Digital Experience Marketing Manager you bring the Ergomed brand to life across three channels: LinkedIn business presentations and our brand websites. Working from the commercial and brand strategy defined by Brand Managers you turn complex ideas and brand messaging into content c...

This is a potential opportunity that may arise at Fortrea in the future. By applying you will join our talent community and be considered for upcoming openings that match your skills and experience.Join Fortrea (sponsor-dedicated) and play a key role in the successful delivery of global clinical tri...

POSITION SUMMARY: Manages ICSR Management Unit for assigned staff and ensures all unit-relevant activities are delivered within agreed extent. Contributes to achieving companys goals and objectives. Performs project budget reviews and provides support to and management of the Associate Directors ICS...

The Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholdersAccou...

Join IQVIA Biotech as a Freelance Clinical Research Associate supporting two Phase III Oncology clinical trials. Youll lead site visits monitor compliance and ensure high-quality dataall while working with a passionate team.Location: Czech Republic travel required (sites are located in Brno Prague O...

The Senior Quality Specialist is primarily responsible for the implementation and maintenance of the quality system and training for their assigned client projects. Thus ensuring that the project maintains compliance with global regulations legislation PrimeVigilance and client requirements.Core res...

The EDC Developer within the ERGOMED Data Management (DM) department is responsible for all tasks linked to the building of the EDC application for complex projects. The EDC Developer represents a position under direction of the Director of Data Management with oversight by the Project Data Manager...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and Functional Service (FSP) solutions.J...

The Manager Regulatory Registration and Compliance is responsible for developing the strategy based on regulatory requirements and for preparing/reviewing relevant Project Plans joint operating procedures and/or templates. They actively assist senior management in securing new business by participat...

ADAMAS Consulting is looking for PV Auditor on a freelance basis to cover audits across Europe. Both full and part time (0.6 FTE) will be considered Planning preparation conduct reporting and follow up (including CAPA plans) of various types of Pharmacovigilance (PV) audits according to expected qua...