Requirements: English
Company: CliniRx
Region: Metropolitan City of Naples , Campania
CliniRx - Clinical Research Associate PositionsCliniRx has multiple CRA positions available to support a global study in Q1 2025. We are expanding rapidly and offer several permanent opportunities to join us on this international project. Ideal candidates will have a background in CROs with experience across various therapeutic areas.As 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, the 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 standards and timelines.Site Management Compliance: Manage sites per the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations.Site Identification: Assist in identifying new potential sites across 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 commitment to quality and adherence to timelines will be crucial for the success of our projects.Key Success FactorsTimely and high-quality execution of site monitoring activities.Prompt reporting and communication with stakeholders.Essential Skills and 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.LocationNapoli, Italia#J-18808-Ljbffr