Clinical Research Associate

US - REMOTE - Contractor or PermAs 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 AustraliaWe are looking to add a number of CRA's in our US operations over the coming Weeks / Months. Interested? Please read on. Primary Purpose:

We are seeking a skilled Site Monitor to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP). Key Responsibilities: Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of 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 within various therapeutic areas to expand our clinical network. Continuous Skill Development:

Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes. Work Relations: Report to the Manager of Clinical Operations for project, functional, and administrative matters. Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative executives. Value Added: Your adherence to the quality and timelines of the monitoring plan will be crucial for the efficient delivery of our projects and overall success. Key Success Factors: Timely and high-quality execution of site monitoring activities. Prompt report generation and submission to stakeholders. Qualifications: 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; ability to multitask and thrive under demanding timelines. Why Join Us?Be a part of a dynamic team at CliniRx that values innovation, collaboration, and excellence. We offer competitive compensation, opportunities for professional growth, and a supportive work environment.