Clinical Research Associate Monitor Senior (m/f)

 

Clinical Research Associate Monitor Senior (m/f) Sorin Group Deutschland GmbH Berlin Planning, organizing, and monitoring clinical studies from initiation to close-out in the areas of Cardiac Rhythm Management (implantable pacemakers, defibrillators, electrodes), Heart Valves and Neuromodulation.

Become A Part Of Our Successful Team In Order To Expand Our Clinical Study Department In Germany Home Based In Berlin Preferably We Are Looking For You To Join Our Team As A Clinical Research Associate Monitor Senior (m/f) Your Tasks: Planning Organizing And Monitoring Clinical Studies From Initiation To Close-out In The Areas Of Cardiac Rhythm Management (implantable Pacemakers Defibrillators Electrodes) Heart Valves And Neuromodulation In Collaboration With National And International Colleagues Preparing And Updating Documentation Reports And Clinical Guidelines Providing Clinical Trial Centers With Advice And Support During Clinical Trials Ensuring Compliance With Trial Protocols And Study-specific Procedures Monitoring And Complying With Quality Management Standards Internal Sops As Well As Budget And Time Allowances Providing Site Start-up And Conduct Support For The Project Management Team Serving As A Reliable Contact Person For Health Authorities Or Ethics Committee As Necessary Mentoring And Training Other Clinical Team Members On Monitoring Processes Your Qualifications: Holding A University Degree In Medicine Biology Or Pharmacy Or Experienced In One Of The Following Roles: Medical Technical Assistant (mta) Pharmaceutical Technical Assistant (pta) Or Nurse Over 5 Years Of Professional Experience As A Clinical Research Associate Monitoring On Sites Clinical Monitoring Experience In Cardiology Preferably In The Area Of Medical Devices Knowledge Of The Respective Laws And Regulations (gcp Cfr ) Good Oral And Written Command In German And English Other European Languages Would Be A Plus Knowledge Of Clinical Software Eg Clinical Trial Management System Electronic Case Report Forms (ecrf) Working Knowledge Of Ms Office Applications And Computer Literate Willingness To Travel On A Frequent Basis Within Europe (a Minimum Of 50%) Ability To Work Independently With Attention To Details And Quality Of Work As Well As Excellent Communication Skills What We Offer: We Offer The Assistance Of An Experienced Team As Well As Supporting You During Your Transition Become A Part Of Our Expanding And Internationally Positioned Company If You Are Interested In This Challenging And Varied Position Then Take The Next Step: Send Us An English Application Stating Your Salary Expectations And Your Earliest Possible Starting Date Via Our Job Portal At: Http://careerslivanovacom We Are Looking Forward To Receiving Your Application Gmbh A Wholly-owned Subsidiary Of Livanova Plc Projektleitung Projektmanagement Projektmanager Biowissenschaften Biologe Referent Referentin Studien CRA CRO Forschung Analyse Naturwissenschaften Dokumantation Naturwissenschaft Medizin Projektleitung Projektmanagement Projektmanager Biowissenschaften Biologe Referent Referentin Studien CRA CRO Forschung Analyse Naturwissenschaften Dokumantation Naturwissenschaft Medizin Clinical Research Associate Monitor Senior (m/f) Planning Organizing And Monitoring Clinical Studies From Initiation To Close-out In The Areas Of Cardiac Rhythm Management (implantable Pacemakers Defibrillators Electrodes) Heart Valves And Neuromodulation Berlin Projektleitung Projektmanagement Projektmanager Biowissenschaften Biologe Referent Referentin Studien CRA CRO Forschung Analyse Naturwissenschaften Dokumantation Naturwissenschaft Medizin

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