Clinical Research Associate In Rome

1 giorno fa


Lazio, Italia Meditrial A tempo pieno

Meditrial is looking for a certified clinical research associate (CRA) experienced in clinical trial monitoring, EDC systems, Digital Health solutions and Data analysis.The resource will participate in the preparation and execution of Phase I-IV clinical trials, oversee the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites.He/she will monitor clinical trials in accordance with Good Clinical Practices and procedures set forth by Meditrial and sponsors.He/she will work closely with the Clinical Project Manager to ensure all monitoring activities are conducted according to study requirements.The resource will be involved in Trial management activities in close collaboration with the CTAs and under the supervision of the Clinical Project Manager.The CRA will be office-based in Rome and be available to travel for monitoring activities.ResponsibilitiesConducting site initiation and investigator trainingReviewing study case report forms (CRFs) completed by the investigative sites, and verifying entries by validating accurate source documentation to support CRF entriesDocumenting site visits and issues in reports and follow-up letters to the siteFacilitating effective communications among investigative sites, the client and MeditrialIdentifying potential investigators in collaboration with the clientResponding to company, client and national regulatory requirements/auditsContributing to the preparation of local forms and documents necessary for Study submissionContributing to the project team by assisting in project communicationsQualificationsHigher or specialized secondary education degree in natural sciencesCRA Certification with monitoring visits are requiredFamiliar with electronic CRF and CTMS systemsIndustry background: CRO/outsourced services, Pharmaceuticals, Biotechnology, Medical DeviceRecent experience in medical device clinical trialsFluency in English and Italian#J-*****-Ljbffr



  • Lazio, Italia Advanced Clinical A tempo pieno

    Senior Clinical Research Associate (Oncology) Working embedded with a leading global oncology-focused biopharmaceutical companyWe are partnering with a top-tier global biopharmaceutical organisation to support a growing oncology portfolio and are seeking an experienced Clinical Research Associate to join the team in an advanced, hands-on clinical role.This...


  • Lazio, Italia Translational Research In Oncology A tempo pieno

    If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.Our passionate team is committed...


  • Lazio, Italia Trio - Translational Research In Oncology A tempo pieno

    Overview If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.Our passionate team is...


  • Lazio, Italia Meditrial A tempo pieno

    A leading clinical research organization in Rome is seeking a certified Clinical Research Associate (CRA) with experience in clinical trial monitoring and data analysis.The CRA will oversee Phase I-IV trials, ensuring compliance with Good Clinical Practices.Responsibilities include conducting site trainings, verifying case report entries, and facilitating...


  • Lazio, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is looking for a certified clinical research associate (CRA) experienced in clinical trial monitoring, EDC systems, Digital Health solutions and Data analysis.The resource will participate in the preparation and execution of Phase I-IV clinical trials, oversee the progress of clinical investigations by conducting site evaluation, initiation, and...


  • Lazio, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is looking for a certified clinical research associate (CRA) experienced in clinical trial monitoring, EDC systems, Digital Health solutions and Data analysis.The resource will participate in the preparation and execution of Phase I-IV clinical trials, oversee the progress of clinical investigations by conducting site evaluation, initiation, and...


  • Lazio, Italia Meditrial Europe Ltd. A tempo pieno

    A leading clinical research organization is looking for a certified Clinical Research Associate (CRA) based in Rome, Italy.The CRA will be responsible for monitoring clinical trials, ensuring compliance with Good Clinical Practices, and conducting site evaluations.Candidates must possess a higher education degree in natural sciences and CRA...


  • Lazio, Italia Translational Research In Oncology A tempo pieno

    If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed...


  • Lazio, Italia Translational Research In Oncology A tempo pieno

    If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed...


  • Lazio, Italia Translational Research In Oncology A tempo pieno

    A global clinical research organization is seeking an experienced Clinical Research Associate to join their team.This home-based position in Italy involves conducting site visits and ensuring compliance with FDA and ICH-GCP regulations.Candidates should have a minimum of 2 years' experience in oncology trials and hold a bachelor's degree in a science-related...