Company: i-Pharm Consulting
Reference: JS - 28112016/2
Closing Date: 12 Dec 16
Salary (£): Negotiable
Clinical Team/Trial Manager REQUIRED FOR A GLOBAL CRO! This is a permanent position for the right candidate to start ASAP!JOB TITLE Clinical Team/Trial ManagerLOCATION BELGIUMNETHERLANDSBENEFITS Competitive Salary Full Benefits Package REQUIREMENTS Bachelor’s degree in a health related field (Master’s degree or PhD is preferred)At least 2 years’ experience as a CTM!Sound knowledge of clinical monitoring procedures Presentation, documentation, and interpersonal skillsFluency in Dutch/French a ...
Clinical Team/Trial Manager REQUIRED FOR A GLOBAL CRO!
This is a permanent position for the right candidate to start ASAP!
Clinical Team/Trial Manager
Full Benefits Package
Bachelor’s degree in a health related field (Master’s degree or PhD is preferred)
At least 2 years’ experience as a CTM!
Sound knowledge of clinical monitoring procedures
Presentation, documentation, and interpersonal skills
Fluency in Dutch/French and English
Performs as project lead for multiservice clinical trials (some global in scope).
Responsible for leading a team of CRAs and managing project coordinators.
Manage the timeline and all project deliverables
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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