Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Were looking for a Clinical Research Associate II (CRA II) to join our growing Clinical Operations team in Italy. If youre passionate about clinical research, enjoy building strong site
Senior Clinical Reseacrh Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Study Start Up Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and
Location:Milan, Lombardy, Italy Job ID: R0140178 Date Posted:2026-08-06 Company Name:HITACHI ENERGY ITALY S.P.A. Profession (Job Category):Engineering & Science Job Schedule: Full time Remote:No Job Description: The opportunity The Service Sales Agreement Specialist will work with the
We are looking for an intern to join our Operations Projects, Quality & Transformation (OPQT) activities. This is a great opportunity to gain experience in a dynamic and international environment while contributing to transformation activities and
Location:Milan, Lombardy, Italy Job ID: R0140779 Date Posted:2026-08-12 Company Name:HITACHI ENERGY ITALY S.P.A. Profession (Job Category):General Management Job Schedule: Full time Remote:No Job Description: The opportunity As BU Risk Management Analyst at Hitachi, Ltd., you will
Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines for the Unblinded model. Assures the implementation of project plans, as assigned. Summary of
Sirio, a premier global aircraft management company, is looking for a Flight Coordination Officer to join our dynamic team. This position will be based at our offices in Milan, Italy. With over 40 years of experience
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary Of Responsibilities Responsible for all
Clinical Research Associate, Sponsor Dedicated – Italy Join to apply for the Clinical Research Associate, Sponsor Dedicated – Italy role at IQVIA Responsibilities Performing site selection, initiation, monitoring and close‑out visits Supporting the development of a subject
Responsibilities Lead high-impact international projects end-to-end, ensuring alignment among global and local stakeholders Manage a portfolio of strategic projects across international markets Prioritize initiatives based on business objectives, ROI, risk, and resource availability Manage brand portfolio
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Job Overview Site monitoring and site
Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study
IQVIA is seeking a scientifically credible and field-based Medical Science Liaison. Youll be the key scientific point of contact for clinical trial sites - supporting site engagement, education, and patient recruitment across a diverse and impactful
BeOne is seeking a Clinical Research Associate to monitor oncology trials across sites in the EU. You will conduct initiation, monitoring, and closeout visits, ensuring data quality and regulatory compliance.Ideal candidates have 3–5 years of CRA experience,
If you are an experienced Senior 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