PCliniRx have a number of CRA positions available to support a global study in Q1 2025. /ppbr/ppWe are expanding at a rapid rate and have multiple opportunities on a permanent basis to join us on a global study. Ideally you will come from a CRO background with experience across multiple therapeutic area's. /ppbr/ppAs a global contract research organization (CRO), we offer a diverse slate of clinical development and resource solutions reflecting both full-service CRO and functional service provider (FSP) models. In supporting clinical outsourcing needs for emerging biotech and pharmaceutical companies—most notably small to mid-size enterprises facing unique challenges we offer our expertise with a presence in key markets including the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia /ppbr/pp------------------------------------------------------------ /ppbr/ppbPrimary Purpose: /b We are seeking skilled CRA's to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP). /ppbr/ppbKey Responsibilities: /b /ppbr/pullibDeliver on the Site Monitoring Plan: /b Gain a comprehensive understanding of the Site Monitoring Master Plan (SMMP), study protocol, and project plan to ensure adherence to quality and timelines. /lilibSite Management Compliance: /b Manage sites according to the SMMP and relevant regulations to minimize Quality Assurance (QA) audit observations. /lilibSite Identification: /b Assist in identifying new potential sites within various therapeutic areas to expand our clinical network. /lilibContinuous Skill Development: /b Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes. /li /ulpbr/ppbWork Relations: /b /ppbr/pulliReport to the Manager of Clinical Operations for project, functional, and administrative matters. /liliCollaborate with the site monitoring team, site personnel, HR, site leads, and administrative executives. /li /ulpbr/ppbValue Added: /b /ppbr/ppYour adherence to the quality and timelines of the monitoring plan will be crucial for the efficient delivery of our projects and overall success. /ppbr/ppbKey Success Factors: /b /ppbr/pulliTimely and high-quality execution of site monitoring activities. /liliPrompt report generation and submission to stakeholders. /li /ulpbr/ppbEssential Skills Experience: /b /ppbr/pullibEducation: /b Bachelor’s or Master’s degree in a scientific discipline. /lilibExperience: /b 1-4 years of experience in site monitoring within clinical research. /lilibSkills: /b Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and thrive under demanding timelines. /li /ul