This leading small sized CRO is seeking an experienced CRA II/ Senior to join their team in Madrid. This is an excellent opportunity to make a real difference and work across Covid studies.
Madrid - Home or Office based
You will have 2.5+ years CRA experience including site selection, routine monitoring and close-out visits. You will have knowledge of and skill in applying clinical research regulatory requirements, GCP and ICH.
This position requires you to perform all clinical site management and monitoring activities including the conduction of qualification visits, site initiation visits and monitoring visits. You will act as the direct contact for assigned clinical sites and will carry out all necessary site documentation verification. You will be required to act as a mentor to other CRA members and to assist them in their training and development.
This globally known and well renowned CRO works on a broad portfolio of trials with this current position focusing on Covid studies.
- Bachelor of Science or Bachelor of Nursing Degree
- 2.5+ years independent monitoring experience
- Thorough knowledge of GCP and ICH
- Strong working knowledge of EDC systems and IVRS is desirable
- Competent in written and oral English and Spanish
- Entitlement to work in Spain
- Full drivers' licence
- Excellent Salary
- Company car or car allowance
- Life Assurance
- 25 days' annual leave
- Flexi Benefits
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. 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.
If you would like to discuss this vacancy further, please call Business Manager Ciara Noble on +44 203 189 0469, or email email@example.com. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / CRA II / Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / England / South England / London / South West / South East / CRO / Contract Research Organisation / Pharmaceutical / Sponsor / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits / Global Pharma / Spain / Madrid /