Research Associate

JR France; Cannes; Sur place; EUR 40 000 - 60 000; Plein temps

Description du poste

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CliniRx have a number of CRA positions available.We 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.As 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------------------------------------------------------------Primary Purpose: 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).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.Essential Skills Experience: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.