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 have 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 offer 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—particularly small to mid-size enterprises facing unique challenges. We have a presence in key markets including 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 accordance 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 enhance technical and soft skills to improve 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 efficient delivery and success 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 of experience in site monitoring within clinical research.Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication skills; ability to multitask and perform under demanding timelines.
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