CRA II - Home or Office Based
About the role
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Job Field: Clinical Operations
Employment Status: Permanent
- You will work within a large-scale, fast-paced international environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate, monitor and close-out investigational sites for clinical studies in phases I to IV, ensuring adherence to applicable SOPs, regulations and principles of ICH-GCP.
- You may assist in training and mentoring fellow CRAs.
- Have existing certification to perform clinical monitoring as per government regulations 2011
- With a University degree in science or equivalent, you have a minimum of 18 months experience as a Clinical Research Associate on clinical studies, all possible therapeutic areas (preferred: TBD per country), in a CRO, Pharma industry or hospital environment.
- You have a driving license and are available to travel throughout Italy.
- Your dynamism, your autonomy, your relationship, your keen sense of organization and your willingness to deliver within required timelines and according to the desired quality, makes you ideally suited to evolve in this function.
- Fluent in English (written, read, spoken).
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
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