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 diverse 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. Our presence includes the USA, UK, the Netherlands, Spain, Hong Kong, India, and Australia. ------------------------------------------------------------ Primary Purpose:
We are seeking skilled CRAs to ensure the timely and quality delivery of site monitoring activities in line 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 for project, functional, and administrative matters. Collaborate with the site monitoring team, site personnel, HR, site leads, and administrative staff. Value Added:
Your commitment to quality and timeliness in monitoring activities is crucial for the efficient delivery of our projects and overall success. Key Success Factors:
Timely, 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 in site monitoring within clinical research. Skills:
Strong understanding of ICH GCP and applicable clinical trial regulations; excellent communication skills; ability to multitask and work under demanding timelines.
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