Company: i-Pharm Consulting
Closing Date: 28 Feb 17
Salary (£): Negotiable
Do you have 1.5 years of CRA monitoring experience? Living in Madrid and looking for a new challenge? I-pharm has an interesting job opportunity for you!
Clinical Research Associate II
Madrid, Permanent contract
The Clinical Research Associate is a health-care professional who performs many activities assuring adherence to GCP-ICH guidelines and company and sponsor SOPs. Preparing for and attending investigator meetings, coordinating and evaluating the quality and integrity of site practices, monitoring dedicated to ONE sponsor with international studies in Oncology and Neurology. This position has ONLY 6-8 visits per month.
A challenging and diversified job in an international setting
Good career opportunities
Excellent team work and management environment
Attractive remuneration up to 43.000€, health and life insurances, ticket restaurant, flexibility, etc
Madrid office based
Your personal qualifications
• Bachelor's degree
• Previous experience in CRO or pharmaceutical company MIN 1.5 YEARS
• Knowledge of ICH and GCP required
• Fluency in written and spoken English
• Position requires to travel
How to apply?
Call to +44 (0) 20 3326 4119 or send me an email firstname.lastname@example.org
If you are looking for a new job opportunity in the pharmaceutical industry, this is the best time to contact me. I work with different clients in Spain who are looking for candidates with different therapies experience in Madrid, Barcelona, Sevilla, Bilbao, Malaga, Valencia. If you are not sure about the market situation. I can provide you with good tips and advices to move forward in your career!
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.
CRA / CRAI / CRA II / CTA / Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / CRA 1 /CRA 2 / ICH-GCP / Clinical Research / Clinical Trials / Study Start-Up / Start-Up / Study Start Up / SSU / Clinical Study Start-Up/ Clinical Study Start Up / Clinical Study Startup / Regulatory Affairs / Regulatory Documents / ICH-GCP / Central Europe / Eastern Europe /Senior CRA / SCRA / Senior Clinical Research Associate / Lead CRA / LCRA / Monitoring / Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / Home Based / Home-Based / Clinical Research / Barcelona / Madrid / Spain / Seville /
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