Local Clinical Research Associate
Job Code: CSA1013A
West (California, Nevada, Arizona) – CV Imaging Device – 4 years
monitoring and 1½ years CV experience
Description
The primary responsibility of this position is to provide site
management, information management, and monitoring of clinical research
studies. Responsibilities may include site monitoring, review of regulatory
documents, accurate and timely documentation and communication, oversight of
safety reporting, development and maintenance of study documents and study
supplies, and management of outside vendors. Travel up to 40% may be
required. Assignment may be based at a client or in the office.
Requirements
Qualified candidates must have an RN or 4-year college degree, preferably
in a biomedical or science related field, and at least 2 years experience as
a Clinical Research Associate.
Skills Required
Understanding of regulatory principles and practices, attention to
detail, ability to efficiently perform multiple tasks, ability to identify
and solve logistical problems, excellent organizational skills, flexibility
with changing priorities, effective communication and personal skills
necessary for successful teamwork. General computer skills with proficiency
in Microsoft Word and Excel are mandatory.
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