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i-Pharm Consulting LtdJoin an international sponsor company to work mainly on Oncology studies. Exciting fully home based option for an experienced CRA located within Greater Copenhagen. LOCATION: home based, Greater Copenhagen SALARY: Negotiable ROLE: * Act as the primary liaison between the CRO and the clinical sites, ensuring the overall integrity of the study implementation and the study protocol at the clinical sites. * Perform on-site visits in accordance with the monitoring plan. * Determine and recommend the appropriate follow-up response to deficiencies in documentation, communication and the need for additional training. * Conduct remote visits, facilities inspections and on-site study training. * Monitor patient safety on an on-going basis and evaluate the overall compliance and performance of sites. * Establish a sit recruitment plan, attend audits and complete routine departmental administrative tasks. * Monitor and maintain ICH-GCP compliance. REQUIREMENTS: * At least two years' independent monitoring experience. Candidate without this experience can unfortunately not be considered. * Ideally candidates will have some oncology exposure. * Educated to a degree level (preferably a health science subject). * Advanced English skills, additional languages would be seen as beneficial. * The successful candidate must be eligible to work in Nordics TO APPLY * Get in touch with Eduard Raudonis on [Phone number removed] * Email [Email address removed] for further information. * If this role is not suitable, Eduard is also available to discuss other possible positions or answer any general questions regarding your career and the current market. ABOUT i-PHARM CONSULTING i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry Globally. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics. [URL removed] KEY WORDS CRA / Monitoring / Pre-study / Initiation / Close-out / Study Start-up / Ethics / Feasibility / GCP / ICH / Clinical Research Associate / Budget Negotiation / / CRA I / CRA II / CRA III / SCRA / Home-based / Contract Negotiation / Site Identification / Science / Pharma / Pharmaceutical / Permanent / SOP / Clinical / Clinical Research Associate I / Clinical Research Associate II / Clinical Research Associate III / On-site / Remote Visits / Study Implementation / Protocol / Site Regulatory Package / Recruitment / Compliance / Patient Safety / CRO / Clinical Research Organisation / Sweden / Denmark / Norway / Finland / Stockholm / Danderyd / Uppsala / Helsinki / Espoo / Vantaa / Copenhagen / Malmo / Lund / Oslo
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