Title
Regulatory Affairs Submissions Coordinator, Regulatory Affairs Submissions Associate, Regulatory Submissions Expert, Regulatory Affairs Submissions Executive, Senior or Level II
Location
Germany, Netherlands, Poland - office based in central locations, details on application
Client
The client is a mid-sized international CRO - ideal for those looking for a change of responsibility and pace of life from larger global CROs. They have been preparing for this massive expansion for many years and are in a stable and secure position now to make a big move in the industry - this is the place to be!
Duties
As Regulatory Submissions Coordinator (II to Senior) you will report to the Regulatory Affairs Manager, key responsibilities will include:
•Distribution, tracking and review of essential trial documentation
•Organisation of regulatory submissions
•Maintenance of timelines for regulatory submissions
•CRA assistance and training for essential documentation throughout clinical trials
•Review, documentation and organisation of TMF
Experience
•Life Science degree
•Pharmaceutical research experience in Regulatory Affairs/ Submissions/ CRA
•Fluent in local languages and English
•Eligible to work in Europe
Salary and Benefits
€30,000 - €45,000 based on experience
Application Process
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
Associated keywords
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