Description
My Client, a leading biotech company is seeking a RA executive to join thier new product developement team for a 9 month contract.Role responsibilities:
*Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.
*Assists in developing procedures to ensure regulatory compliance.
*Has knowledge of commonly-used concepts, practices, and procedures within a particular field.
*Relies on instructions and pre-established guidelines to perform the functions of the job.
*Role is focused on coordinating and compiling submissions for EU and Emerging Markets
Candidate Background:
*Experience in a regulated industry, science academia or clinical practice.
*Educated to degree level or equivalent
*At least 2 years experience in regulatory affairs in Europe or the UK with experience of submissions to regulatory bodies
*Some experience of CMC aspects of clinical trials submissions would be an advantage
If this role sounds like an ideal match for your experience and/or career motivations, please contact me Anna Mooney or apply below with an updates CV.
To find out more about Real please visit www.realstaffing.com