Requirements: English
Company: CliniRx
Region: Modena , Emilia-Romagna
Job Title: Clinical Research AssociateLocation: Modena, ItaliaOverviewCliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer numerous permanent opportunities to join our team on a global scale. Ideal candidates will have a background in CROs with experience across various therapeutic areas.About UsAs a global contract research organization (CRO), we provide a diverse range of clinical development and resource solutions, including full-service CRO and functional service provider (FSP) models. We support clinical outsourcing for emerging biotech and pharmaceutical companies, especially small to mid-size enterprises facing unique challenges. Our presence spans key markets including the USA, UK, Netherlands, Spain, Hong Kong, India, and Australia.Primary PurposeWe are seeking skilled CRAs to ensure the timely and high-quality delivery of site monitoring activities in accordance with our Site Monitoring Plan (SMP).Key ResponsibilitiesDeliver on the Site Monitoring Plan: Understand the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality 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 enhance technical and soft skills to improve performance and project outcomes.Work Relations: Report to the Manager of Clinical Operations and collaborate with site monitoring teams, site personnel, HR, site leads, and administrative staff.Value AddedYour adherence to quality standards and timelines is crucial for the successful delivery of our projects.Key Success FactorsTimely and high-quality execution of site monitoring activities.Prompt report generation and submission to stakeholders.Essential Skills & ExperienceEducation: Bachelors or Masters degree in a scientific discipline.Experience: 1-4 years in site monitoring within clinical research.Skills: Strong understanding of ICH GCP and clinical trial regulations; excellent communication skills; ability to multitask under demanding timelines.#J-18808-Ljbffr