Company: i-Pharm Consulting
Closing Date: 12 Dec 16
Salary (£): Negotiable
Clinical Project Manager REQUIRED FOR A GLOBAL CRO! This is a permanent position for the right candidate to start ASAP!JOB TITLE PM II, senior PMLOCATION BELGIUMOffice basedHome basedBENEFITS Competitive Salary Full Benefits Package REQUIREMENTS BA/BS in the life sciencesAt least 3 years experience as a PM PM role in a CRO is strongly desiredAt least 2 years Ophthalmology experience preferred in Regional Studies or Global StudiesSound knowledge of regulatory requirements, drug or device deve ...
Clinical Project Manager REQUIRED FOR A GLOBAL CRO! This is a permanent position for the right candidate to start ASAP!
PM II, senior PM
Full Benefits Package
BA/BS in the life sciences
At least 3 years experience as a PM
PM role in a CRO is strongly desired
At least 2 years Ophthalmology experience preferred in Regional Studies or Global Studies
Sound knowledge of regulatory requirements, drug or device development, and clinical monitoring procedures
Presentation, documentation, and interpersonal skills
Fluency in Dutch/French and English
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 Principal Consultant Josette Shikayi able, Josette is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
CRA / CRAI / CRA II / CTA / / SCRA / Monitoring /Monitor / Clinical Trial / Drug Trial / Trial Sites / Clinical / CRA 1 /CRA 2 / ICH-GCP / Clinical Research / Clinical Trials / Study Start-Up / SSU / Clinical Study Start-Up/ Start-up / Regulatory Affairs / Regulatory Documents / ICH-GCP / Central Europe / Eastern Europe / Clinical / Home Based / Office Based / Clinical Research / Antwerpen / Brussels / Gent /Eindhoven/Belgium
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