CRA II/Senior CRA
2 giorni fa
What you will be doingConducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports.Your profileBachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Ability to travel at least 60% of the time (international and domestic – fly and drive) and possess a valid driver’s license.What ICON can offer you Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being. Life assurance Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply. #J-18808-Ljbffr
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CRA II
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Milan, Italia ICON A tempo pienoCRA II / Senior CRA ICON Biotech ICON 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 development. We are currently seeking a Senior Clinical Research Associate...
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Senior CRA
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Milan, Italia ICON A tempo pienoSenior CRA / CRA II ICON 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 development. We are currently seeking a Senior Clinical Research Associate (CRA) to join...
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Senior CRA
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Milan, Italia ICON A tempo pienoSenior Clinical Research Associate - France - Remote ICON 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 development. We are looking for motivated CRA II or...
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Home-Based CRA II/III – Oncology, Italy
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Senior CRA
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Senior Clinical Research Associate
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Milan, Italia ICON A tempo pienoA global clinical research organization is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trials and ensure compliance with regulatory standards. The successful candidate will have extensive experience in clinical trial processes and strong organizational skills. Responsibilities include monitoring sites, conducting visits, and...
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Clinical Research Associate II/III
4 giorni fa
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Clinical Research Associate II/III
4 giorni fa
Milan, Italia Optimapharm A tempo pienoLocation: located in North Italy; MilanWho we are?Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients’ lives.Optimapharm’ s key priorities are the well-being of our people, consistent quality delivery to our clients and healthy, sustainable growth.With 26 strategically...
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Clinical Research Associate II/III
6 giorni fa
Milan, Italy (Remote) Optimapharm . A tempo pienoLocation: located in North Italy; MilanWho we are?Optimapharm is a globally operating, leading, mid-sized, full-service CRO aiming to deliver new therapies to improve and save patients' lives. Optimapharm' s key priorities are the well-being of our people, consistent quality delivery to our clients and healthy, sustainable growth.With 26 strategically...
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Senior Clinical Research Associate – Israel
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Milan, Italia ICON A tempo pienoA leading healthcare intelligence organization is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Milano, Italy. The role involves monitoring clinical trial sites, collaborating with diverse teams, and ensuring compliance with regulatory requirements. The ideal candidate will have an advanced degree in a relevant...