Mid-size global CRO - ideal for those looking for a change of responsibility and pace of life from LARGE CROs - move to a growing midsize company and enjoy being part of exciting growth!
•Regulatory Submissions Coordinator
•Start-Up Specialist / Associate
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
Location: Belgium / France / UK
Salary: €25,000 - €40,000 based on experience
SKILLS REQUIRED
•Life Science degree
•Pharmaceutical research experience in Regulatory Affairs/ Submissions/ CRA
•Fluent in local languages and English
•Eligible to work in Europe
A rapidly growing, exciting Contract Research Organisation!
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: Senior CRA, Senior Clinical Research Associate, Senior Monitor, CRA II, CRA III, Clinical Research Associate II, CRO, Pharmaceutical, Biotech, Belgium, Wavre, Mechelen, Leuven, France, Lyon