Clinical Research Associate

2 settimane fa

Milano, Italia JR Italy A tempo pieno

Social network you want to login/join with: CliniRx has a number of CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer multiple permanent opportunities to join us on a global study. Ideally, candidates will come from a CRO background with experience across multiple therapeutic areas. As a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, reflecting both full-service CRO and functional service provider (FSP) models. We support clinical outsourcing needs for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges. Our presence includes the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia. ------------------------------------------------------------ Primary Purpose: We are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in line with our Site Monitoring Plan (SMP). Key Responsibilities: Deliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality standards and timelines. Site Management Compliance: Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations. Site Identification: Assist in identifying new potential sites across various therapeutic areas to expand our clinical network. Continuous Skill Development: Regularly improve technical and soft skills to enhance performance and project outcomes. Work Relations: Report to the Manager of Clinical Operations regarding project, functional, and administrative matters. Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff. Value Added: Your adherence to quality standards and timelines in monitoring activities is crucial for the successful delivery of our projects. Key Success Factors: Timely and high-quality execution of site monitoring activities. Prompt report generation and submission to stakeholders. Education: Bachelor’s or Master’s degree in a scientific discipline. Experience: 1-4 years in site monitoring within clinical research. Skills: Strong knowledge of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills; ability to multitask and perform under demanding deadlines. #J-18808-Ljbffr

  • Clinical Research Associate

    4 settimane fa

    Milano, Italia Medpace A tempo pieno

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    1 settimana fa

    Milano, Italia Altro A tempo pieno

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    Milano, Italia Altro A tempo pieno

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    Milano, Italia Medpace A tempo pieno

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    Milano, Italia CROMSOURCE A tempo pieno

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    2 settimane fa

    Milano, Italia IQVIA A tempo pieno

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