Clinical Study/Trial Manager - Leading Medical Device Org - NL

Provincie Overijssel  ‐ Onsite
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Description

Clinical Study/Trial Manager - Netherlands - Pharmaceutical Org.
Project Management, Support, Coordinator, Project Manager, CRA, Research, Study, Medical Devices,Drug delivery, Drugs, Clinical Studies, Research, Trials, Project Manager, Project Leader, Continuous Improvement, Service Orientated, Stakeholder Management, Senior, Dutch, English, Biotech, Pharmaceuticals, CRO, Post market, Registration, Monitoring, FDA Audits, FDA, Monitor, Protocols, Site Selection, Initiation.
My client needs a Clinical Trial/Study manager, who is hands-on, experienced and can work across a European Study from Site selection to FDA Audits. You will provide a supporting/coordinating role - working closely with the European Study Lead to drive a project through.
-Proactive
-Flexible
-Good Project Management skills
-Solid CRA exposure, Good Clinical Research & Study/trial management experience
-Excellent pharmaceutical/life science/Medical Device background
My client needs a confident, strong, outgoing communicator to play a key role with clients (physicians/doctors/senior medical professionals) as an experienced CSM (Clinical Study Manager) with good Research & Study exposure.
An exciting opportunity for a Senior European Trial Lead with good research and trial knowledge to join one of the leading organisations of its type globally. My client needs someone who can coordinate, lead, organise and also demonstrate reasonable awareness of CRA responsibilities/skills.
Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.
Start date
n.a
From
Amoria Bond - UK
Published at
22.09.2016
Project ID:
1207460
Contract type
Freelance
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