Description
We are currently working alongside a global top 10 CRO who are searching for a regulatory specialist to join their team on a contract basis.Job details & description:
As a member of our Study Start Up team you will traverse all therapeutic areas and phases, providing your expertise at this vital period of time in the study Industry standard.
They are currently looking to strengthen the Ethics and Regulatory department and are seeking an experienced Senior SSU & Regulatory Specialist.
A brief summary of duties you will be involved in as a Senior Site Start up Specialist
- Reviewing essential document packages for site activation
- Preparation and submitting of Central EC Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required
- Reviewing Informed Consent Forms
Qualifications Needed:
- Previous experience in clinical research including submissions experience
- Knowledge of local regulatory requirements/guidelines, such as Code of Federal Regulations and European Union Directive as well as any applicable rules applicable locally.
If you are interested please let me know and I will forward you more details. Alternatively if you know anyone who may be interested in this role please pass on these details. Any successful referral is entitled to £200 vouchers.
To find out more about Real please visit www.realstaffing.com
Real Staffing, a trading division of SThree Partnership LLP | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales