04/02/2013
We zijn per direct op zoek naar: Clinical Research Associate, Engeland
The Company
Our Client, a leader in medical products and software solutions, helps responders manage, treat, and save lives in emergency rescues and in hospitals; outside the hospital while at work or home; in doctors' and dentists' offices and schools; in public places and on the battlefield. Our client's products contribute to managing patient care and saving lives, as well as increasing the efficiency of emergency medical, fire, and hospital operations around the globe.
The Position
Assists in the design, planning and conduct clinical research trials by effectively coordinating the activities of study coordinators and investigators and by ensuring compliance with study protocols, US and/or EU regulations, IRB/EC requirements and overall clinical objectives.
Our Expectations
• Two to five years related experience in coordinating multi-center clinical trials. Cardiac, critical care, ED or neuro background is preferred. Monitoring experience required.
• Working knowledge of FDA/EU regulatory requirements.
• Working knowledge of clinical trial site budget, contracts and payments.
• Requires travel up to 75%.