Company: i-Pharm Consulting
Closing Date: 28 Feb 17
Salary (£): Negotiable
Do you have at least 2 years' experience as a Clinical Research Associate? Do you have experience in a CRO for over 1 year?If you've answered YES to any of the above questions, then i-Pharm might have the right role for you!
Do you have at least 2 years’ experience as a Clinical Research Associate? Do you have experience in a CRO for over 1 year?
If you’ve answered YES to any of the above questions, then i-Pharm might have the right role for you!
Clinical Research Associate (CRA)
-Conduct the clinical monitoring aspects of designated projects.
-Perform clinical on-site monitoring activities
-Collect regulatory documentation
-Perform qualification, initiation, monitoring and close out visits
-You will function as the primary contact for sites
-You will be a key member of the Clinical Operations team
-This position may require domestic and international travel
Fluency in written and spoken English
Fluency in written and spoken Hungarian
Life Science degree would be preferable
Previous experience as a CRA
Strong time management skills
WHAT WE OFFER:
-Home or Office based position
-Competitive salary package + other benefits
-Possibility to manage your own projects
-Possibility to progress to a Team Leader position
-Friendly work atmosphere
How to apply?
Please apply here on send your CV to : firstname.lastname@example.org
If you have any questions please send an email to email@example.com
You can also call us on : +4402031890467
Not the right role?
We are always happy to discuss in more detail about other opportunities we might have available and consult you. If you're thinking to change but not sure about the market, we are always there to keep you informed with the latest news and greatest opportunities.
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 / Hungary/ Budapest
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