Requirements: English
Company: CliniRx
Region: Rimini , Emilia-Romagna
CliniRx have a number of CRA positions available tosupport a global study in Q1 2025. We are expanding at a rapid rateand have multiple opportunities on a permanent basis to join us ona global study. Ideally you will come from a CRO background withexperience across multiple therapeutic area''s. As a global contractresearch organization (CRO), we offer a diverse slate of clinicaldevelopment and resource solutions reflecting both full-service CROand functional service provider (FSP) models. In supportingclinical outsourcing needs for emerging biotech and pharmaceuticalcompaniesmost notably small to mid-size enterprises facing uniquechallenges we offer our expertise with a presence in key marketsincluding 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.