Clinical Research Associate

17 ore fa

Rovigo Provincia di Rovigo, Italia Pivotal A tempo pieno

Pivotal is excited to expand our team and we are looking for an experienced, highly motivated Clinical Research Associate who shares our vision of providing clinical research excellence.
Joining Pivotal as a CRA/SCRA means that you’ll enjoy being a member of one of the leading full-service contract research organizations in Europe with a very solid reputation. This role promises to gain direct experience with our clients and offer career growth and professional development within a scientific and data driven company. You’ll have the opportunity to put your passion to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
We are passionate and fully committed with medical science while using technology, to make a positive impact
We take care of our employees and we ensure everyone receives permanent mentoring and training and a push to always take one step further as well as untold international experience that will help you grow and will accompany all your life
Be part of multi-national project teams and focus on delivering exemplary levels of customer service on multiple, challenging studies
Perform site selection, initiation, monitoring and close-out visits
Collaborate with the Regulatory team to obtain Ethic Committees (ECs) and Health Authorities (HAs) approvals in accordance with national/international regulations
Evaluate the quality and integrity of site practices in accordance with regulatory requirements, i.e., immediately communicates/escalates serious issues to the project team and develops action plans
Manage site progress by tracking recruitment, eCRF completion, and data query resolution
Participate in problem-solving and risk-mitigation strategies
University Degree in life science or other scientific discipline or apprenticeship in health care
Minimum of two years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
Knowledge of applicable clinical research regulatory requirements i.e., Flexibility to travel 6-8 visits per month
Fluency in Italian and English
Good knowledge of Office (Word, Excel and PowerPoint)
Leaders that support flexible work schedules
Trainings to help you build your therapeutic knowledge

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