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Clinical Research Associate with Global Expertise
hace 1 mes
We are seeking a highly skilled Clinical Research Associate to join our team at Boston Scientific. This is an exciting opportunity for individuals who are passionate about advancing medical science and improving patient lives.
Key Responsibilities:- Clinical Trial Site Start-up Activities: Work independently to coordinate all necessary activities for site regulatory submissions and essential document collection for allocated clinical research sites.
- Regulatory Document Management: Manage multiple sets of essential regulatory documents across several studies and division portfolios.
- Site Relationships: Develop and foster clinical research site relationships to become a subject matter expert in the site start-up regulatory process across multiple studies.
- Bachelor's Degree or equivalent experience and education.
- Experience in study submissions to the Ethics Committee (Spain or Italy).
- Fluency in English, Italian, and Spanish.
- Ability to multi-task and work in a fast-paced environment.
- Research Coordinator or In-House Clinical Research Associate / Clinical Research Associate / Study Start-up Specialist experience.
- Experience working with Ethics Committees.
- Experience working with clinical trial management systems (e.g., Siebel CTMS, Veeva) and clinical document control systems/eTMF.
We are committed to solving the challenges that matter most united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate.
What We Offer:We offer a competitive salary range of approximately €60,000 - €80,000 per year, depending on location and experience.
