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KeyPartners Italy è una società di ricerca e selezione del personale e advisory HR, specializzata nell'individuazione di profili ad alta specializzazione per aziende nazionali e internazionali. · Operiamo con un approccio consulenziale e data-driven, affiancando i clienti nella c ...
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KeyPartners Italy è una società di ricerca e selezione del personale e advisory HR, specializzata nell'individuazione di profili ad alta specializzazione per aziende nazionali e internazionali. · Operiamo con un approccio consulenziale e data-driven, affiancando i clienti nella c ...
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The Clinical Research Associate will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct. · ...
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The Clinical Research Associate (CRA) is a member of the Project Team and is responsible for the initiation, on–site and/or remote monitoring, close out of study sites during study conduct. · ...
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Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. · ...
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If you are an experienced CRA who is passionate about oncology research TRIO is the place for you · Conducting site visits including pre-study initiation monitoring and termination; · Confirming adherence to all FDA ICH-GCP and local regulations; · ...
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We are looking for a Clinical Research Associate to join our Monitoring Resources team. Reporting to a CRA Line Manager, this position will be home-based in Italy. · This position involves conducting site visits, · confirming adherence to all FDA regulations, · and ensuring imple ...
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The Clinical Research Associate is part of Clinical Development Services (CDS) or Strategic Resourcing Solutions (SRS) within TFS Health Science and will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, ...
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The Clinical Research Associate is part of Clinical Development Services (CDS) or Strategic Resourcing Solutions (SRS) within TFS Health Science and will function operationally as a member of a Project Team. · Monitor on-site and remotely clinical trials in accordance with TFS an ...
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· 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 clinical research organization dedicated to advancing ...
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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 · ...
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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 clinical research organization dedicated to advancing tran ...
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Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. · ...
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We are looking for a Senior Clinical Research Associate to join our Monitoring Resources team. · ...
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Meditrial is looking for a certified clinical research associate (CRA) experienced in clinical trial monitoring. · ...
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A Clinical Research Associate II will be responsible for managing clinical trials and ensuring compliance with regulatory requirements at investigational sites. They will also train and motivate site staff to achieve trial goals. · ...
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Clinical Research Associate I - Roma - ICON Strategic Solutions
Descrizione
Clinical Research Associate II
Dato che un elevato numero di candidati potrebbe essere interessato a questa posizione, si assicuri di inviare il suo CV il prima possibile.
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 Clinical Research Associate II to join our diverse and dynamic team.As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
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 profile
Bachelor's degree in a scientific or healthcare‑related field.
Minimum of 2 years of experience as independent Clinical Research Associate and certified as per Italian DM.
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 should possess a valid driver's license.
What ICON Can Offer YouOur 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.
Our Benefits Examples IncludeVarious 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, subsidized 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? xkiyazw Please click here to apply.#J-18808-Ljbffr
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