Add

Senior Regulatory Affairs Associate - UK or Italy

Lead the coordination of our Global Regulatory Projects and gain the international clinical trials experience that you career deserves.

The need to co-ordinate and prepare submissions to various international authorities and ethics committees, along with the ability to handle regular contact with internal teams and clients means this opportunity would suit an experienced regulatory professional seeking to further develop their regulatory skills.

i3 Research, a UnitedHealth Group Company, is a full-service, global clinical research organization therapeutically focused on: central nervous system, oncology, respiratory and infectious diseases, endocrinology and metabolic diseases, and cardiology. i3 brings sharp therapeutic focus to clinical research, while providing global reach. With 47 offices worldwide we have the resources to launch clinical trials in virtually any location.

You will need a Bachelor’s level degree in life sciences, pharmacy or a suitable equivalent qualification as well as demonstrated regulatory affairs experience gained in either Pharmaceutical, Biotechnological or Clinical Research organisations. Recent experience of clinical trials applications (CTA’s) to Ethics Committees would be highly desirable.

If you have the energy, enthusiasm and drive to work in our fast-paced international environment then we would like to hear from you.

Please apply to colin.grugeon@i3global.com or for an informal chat call me directly in confidence Tel +44 (0)1628 408532


Regulatory Affairs Associate / Senior Regulatory Affairs Associate / Regulatory Affairs / Regulatory Affairs / Regulatory Affairs / Team Leader / Clinical / Clinical / Clinical / Pharmaceutical / Pharmaceutical / Clinical Trials Application / CTA / CTA / IMPD / IMPD / CMC / CMC / International / Maidenhead / Maidenhead / Berkshire / Berkshire / London / London / South East / South East /