Regulatory Affairs Associate

Charing Cross Station
£35000 - £45000 per annum + competitive
08 Nov 2017
13 Dec 2017
Contract Type
Full Time
A biotechnology company in London are looking for a Regulatory Associate. If you can demonstrate significant pharmaceutical experience, then you could be the Regulatory Associate that were looking for.

What will you be doing?

As a Regulatory Associate, youll effectively execute a regulatory strategy. Youll be the principle point of contact for EEA regulatory authorities for IMPD submissions and will effectively prepare US INDs and IND maintenance. Furthermore, youll implement the preparation of meeting materials for US and EEA regulatory authority meetings. If you have the ability to provide quality assurance leadership, then we want to hear from you!

What skills/experience should you have?

Significant regulatory affairs experience in the pharmaceutical industry
Experience of submission execution (IND, IMPD, FDA, CDER)
Knowledge of regulatory strategy

Who will you be working for?

As a Regulatory Associate, youll be working for a highly respected biotechnology company in London. Youll be joining a small team in a business that offers you the opportunity to get involved in various aspects of the organisation. Furthermore, youll also be offered flexible working options.

Do you want to join an organisation that really offers you the opportunity to make a difference? If so, get in touch, today!

Sthree UK is acting as an Employment Agency in relation to this vacancy. Advertised through Zoek 4fabab4aea8b49ec8838e045aa5f44e98