The experienced Senior Clinical Research Associate (CRA) Home Base performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA/EMEA/ and preferably some knowledge of Latin America/South American local guidelines, local regulations and ESTERN Medical Standard Operating Procedures and experience. Experience in Pharmaceuticals / Medical Devices.
The Sr. CRA will conduct site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents ESTERN Medical in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel. May assist project manager or clinical team manager on assigned projects and/or may assist in the mentoring and training of junior clinical team. Required to travel 25-50%