Description
You will be responsible for the overall execution of small-medium regulated and non-regulated clinical projects or large non-regulated clinical projects. These will include ( but are not limited to) study planning, initiation, budget tracking, tracking and supporting subject recruitment, monitoring, quality of deliverables, site support and study closure. You will also be working closely with all parties involved in executing a clinical study.You will have one or more of the following experience/skills:
* Minimum of a Bachelor's Degree, preferably in a Life Science, Physical Science, Nursing, or Biological Science.
* BS with at least 3 years of relevant experience preferred. * Previous experience in clinical study management or equivalent is required. * Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
* Clinical/medical background a plus.
* Medical device experience a plus.
* Basic skills in project management.
* Understanding of Good Clinical Practices.
* Understanding and application of regulations and standards applied in clinical areas is required.
If you are interested in this opportunity and want to work for one of the world's largest multinational pharmaceutical and biotechnology companies, please forward your CV or for further information, you can contact me on the details below. If this role isn't for you, but you know of someone who would be interested, we offer £200 in vouchers through our referral scheme so what are you waiting for!
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