Regulatory Submissions Coordinator

Lyon, Auvergne-Rhône-Alpes, FR
07 Jan 2021
06 Feb 2021
Regulatory Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Job Summary
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the clinical trial management process. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

*Make sure that submissions are compliant with local regulations
*Prepare, review and send the submissions to relevant authorities and file them
*Review pertinent regulations to develop proactive solutions to start-up issues and challenges and advise sponsors accordingly
*Follow the submissions and make sure documents are filed in the required time lines

*A Bachelor's degree in life sciences or biology;
*At least 2 years of experience in preparing, reviewing and submitting regulatory documents
*Strong oral and written communication skills;
*Fluency in English
*Excellent computer skills, including a working knowledge of Microsoft Office applications

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