Clinical Research Associate, Sponsor Dedicated

3 giorni fa


Milano, Lombardia, Italia IQVIA A tempo pieno 50.000 € - 80.000 € all'ano

Experienced Clinical Research Associate, Italy

Your responsibilities will include:

  • Performing site selection, initiation, monitoring and close-out visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
  • Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
  • Collaborating with experts at study sites and with client representatives

Qualifications:

  • University Bachelor's Degree and Master's Degree in scientific discipline or health care
  • In possession of CRA Certification as required by Ministerial Decree dated
  • Experience in Pharma Industry, and/or Clinical Trials environment
  • Very good computer skills including MS Office
  • Excellent command of English language
  • Organizational, time management and problem-solving skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
  • Flexibility to travel
  • Driver's license class B

What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Excellent working environment in a stabile, international, reputable company
  • Company car, mobile phone and attractive benefits package

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more



  • Milano, Lombardia, Italia ICON plc A tempo pieno 80.000 € - 120.000 € all'ano

    Clinical Research AssociateICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Clinical Research Associate - Cell Therapy...


  • Milano, Lombardia, Italia MCR - Mediolanum Cardio Research s.r.l. A tempo pieno 30.000 € - 60.000 € all'ano

    Mediolanum Cardio Researchèalla ricerca di un/a Clinical Research Associate (CRA) certificato/adi talento e motivato/a per unirsi al nostro team di ricerca clinica.Responsabilità PrincipaliIl candidato ideale sarà responsabile della gestione e del monitoraggio delle attività degli studi clinici in conformità con i protocolli di ricerca, le Good...


  • Milano, Lombardia, Italia ICON plc A tempo pieno 45.000 € - 65.000 € all'ano

    Senior CRA / CRA IIICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical Research Associate (CRA) to join our...


  • Milano, Lombardia, Italia IRE A tempo pieno 45.000 € - 55.000 € all'ano

    CRA II / Senior CRA ICON BiotechICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical Research Associate (CRA)...


  • Milano, Lombardia, Italia Syneos Health A tempo pieno 45.000 € - 65.000 € all'ano

    DescriptionSponsor dedicated Sr CRA I - Home Based ITASyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the...


  • Milano, Lombardia, Italia Medpace A tempo pieno 40.000 € - 80.000 € all'ano

    The Clinical Research Associate position at Medpace offers the unique opportunity to have anexciting careerin the research of drug and medical device development whilemaking a differencein the lives of those around them. For those with amedical and/or health/life science backgroundwho want to explore the research field and be part of a team bringing...


  • Milano, Lombardia, Italia PSI CRO A tempo pieno 35.000 € - 55.000 € all'ano

    Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate at PSI...


  • Milano, Lombardia, Italia IQVIA A tempo pieno 40.000 € - 80.000 € all'ano

    Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions:• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...


  • Milano, Lombardia, Italia OPIS Research A tempo pieno 24.000 € all'ano

    Are you a clever, proactive, and detail-oriented individual ready to start your finance career? OPIS Italy is looking for an Accounts Receivable Associate to join our Finance team near Desio HQ. This is your chance to grow professionally, work closely with experienced finance professionals, and make an impact in a dynamic, supportive environment.Location:...


  • Milano, Lombardia, Italia IQVIA A tempo pieno 40.000 € - 80.000 € all'ano

    Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.Essential FunctionsComplete appropriate therapeutic, protocol and clinical research...