Requirements: English
Company: CliniRx
Region: france, fr ,
CliniRx have a number of CRA positions available. Weare expanding at a rapid rate and have multiple opportunities on apermanent basis to join us on a global study. Ideally you will comefrom a CRO background with experience across multiple therapeuticarea''s. As a global contract research organization (CRO), we offera diverse slate of clinical development and resource solutionsreflecting both full-service CRO and functional service provider(FSP) models. In supporting clinical outsourcing needs for emergingbiotech and pharmaceutical companiesmost notably small to mid-sizeenterprises facing unique challenges we offer our expertise with apresence 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 timelyand qualitative delivery of site monitoring activities in alignmentwith our Site Monitoring Plan (SMP). Key Responsibilities: -Deliver on the Site Monitoring Plan: Gain a comprehensiveunderstanding of the Site Monitoring Master Plan (SMMP), studyprotocol, and project plan to ensure adherence to quality andtimelines. - Site Management Compliance: Manage sites according tothe SMMP and relevant regulations to minimize Quality Assurance(QA) audit observations. - Site Identification: Assist inidentifying new potential sites within various therapeutic areas toexpand our clinical network. - Continuous Skill Development:Regularly enhance both technical and soft skills, applying them toelevate performance and project outcomes. Work Relations: - Reportto the Manager of Clinical Operations for project, functional, andadministrative matters. - Collaborate with the site monitoringteam, site personnel, HR, site leads, and administrativeexecutives. Value Added: Your adherence to the quality andtimelines of the monitoring plan will be crucial for the efficientdelivery 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: Bachelors or Mastersdegree in a scientific discipline. - Experience: 1-4 years ofexperience in site monitoring within clinical research. - Skills:Strong understanding of ICH GCP and applicable clinical trialregulations; excellent verbal and written communication; ability tomultitask and thrive under demanding timelines.