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We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials.
The Clinical Research Associate will manage multiple aspects of subjects' welfare. You will conduct regular site visits, generate and distribute internal and external newsletters, prepare final reports and liaise with interested parties regarding all trial aspects.
You will play a leading role in generating and overseeing documentation and records.
To be successful in this role, you should be able to recognize logistical problems, and initiate appropriate solutions.
Ideal candidates will be detail-oriented, have the ability to multitask and be able to collaborate with various role players.
Job Summary
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