- Clinical Trial Specialist
- Submissions Specialist
- Start-up Associate
- Regulatroy Coordinator
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This leading global CRO with offices in Netherlands can offer you home/office flex, reward experience with top salarys and help you meet your development goals
ROLE RESPONSIBILITIES:
Update tracking systems, follow up on site related queries and submit documentation to satisfy safety updates, as well as completing routine administrative tasks in a timely manner. The role expects:
• Produce country specific Informed Consent Forms
• Data entry and maintenance
• Project-specific site selection at a National level
• Collaborate with CRA’s in compiling regulatory documentation
SKILLS DESIRED:
• Submissions experience (local laws)
• Proficient regulatory knowledge (GCP)
• Life sciences degree, Nursing qualification or other relevant experience
• Fluent English and Dutch essential
Location: Netherlands, Amsterdam
Salary: €27,000 – 45,000 (based on experience)
Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com
Contact via LinkedIn: http://uk.linkedin.com/in/craigedwardsmeet
Meet are good people who are great at recruitment. We're proud to partner with the industry's leading Pharmaceutical and Healthcare companies, helping them find and secure the best global talent available
Find out more about Meet at www.peoplewithchemistry.com