Study Manager Jobs in Poland

Job OverviewThe Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations Study Management to time cost and quality from Clinical Study Protocol (CSP) development through study set-up maintenance close-out...

Job OverviewThe Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations Study Management to time cost and quality from Clinical Study Protocol (CSP) development through study set-up maintenance close-out...

When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...

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...

Associate Director Project Data ManagerLocation: WarsawJob Description / CapsuleResponsible for the oversight of the Clinical Data Management (CDM) delivery of high-quality data via external partners or internally run studies for one or more assigned projects or an indication. Alternatively acts as...

Labcorp is seeking a remote Global Study Manager (1year contract) to join our team in Poland.Work schedule: Monday - FridayJob Responsibilities:Key contact for clients; Liaison between Clients CRO and LabcorpDisplays leadership to ensure successful interactions between LabCorp study team members nee...

WE ARE BUILDING PIPELINE OF CANDIDATES - THIS IS NOT ACTIVE RECRUITMENTIn AstraZenecas Cell Therapy division we follow the science to explore and innovate. We are working towards treating preventing modifying and even curing some of the worlds most complex diseases. We have the potential to grow our...

As a CRA you will have local responsibility for the delivery of the studies at allocated sites and you will be an active participant in the local study team(s). You will work in close collaboration with other CRAs and the Local Study Team/ Local Study Manager to ensure that study commitments are ach...

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...

Labcorp is seeking a remote Study Design Lead to join our Central Labs Services team in Poland.Job ResponsibilitiesAccurately interpret and translate sponsor protocol requirements into the protocol specific database to generate a Statement of Work for the CLS project.Leverage technical therapeutic a...

Study StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 3- 6 monthsAre you an experienced Regulatory & StartUp professional looking to lead complex clinical trial startu...

Associate Study StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 4-6 monthsAre you looking to take the next step in your Regulatory & StartUp career within clinical res...

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...