Tipo de jornada
Sin especificar
Tipo de contrato
Sin especificar
Estudios mínimos
Sin especificar
Descripción del empleo
This leading, international CRO is seeking a clinical research profession with 2+ years' monitoring experience to work across a range of complex therapy areas. This is a single sponsor model and therefore you will get the opportunity to work directly with a top pharma company. This pharma offers a strong management structure in order to provide CRA's with a better support system and therefore better work-life balance.
LOCATION
Home Based - Madrid or Barcelona
RESPONSIBILITIES
- Conduct site initiation visits, routine monitoring visits, and close-out visits
- Liaise with the PI and site staff
- Apply research regulatory requirements, GCP and ICH.
- Possess strong communication skills - to present findings at investigator meetings and to discuss budgets with potential investigators
REQUIREMENTS
- Bachelor of Science or Bachelor of Nursing Degree
- 2+ years monitoring experience
- Entitlement to work in Spain
- Fluent Spanish
BENEFITS
- Excellent Salary
- Car allowance
- Healthcare
- 25 days' annual leave
- Pension
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.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Recruitment Consultant Ciara Noble on +44 (0)20 31890469, or email cnoble@i-pharmconsulting.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.
KEY WORDS
CRA / CRA II / Clinical Research Associate / SCRA / Senior Clinical Research Associate / Clinical Monitor / Clinical Trials / Phase I / Phase II / Phase III / Phase IV / Good Clinical Practice / GCP / Oncology / CNS / Spain / Madrid / Barcelona / Home-Based/ Pharma's / Major Pharma's / Sponsor Pharma's / CRO / Contract Research Organisation / Pharmaceutical /Multiple Sponsors / Home Based / Study Start-Up / Feasibility / Site Identification / Site Initiation / Routine Monitoring / Close Out Visits /