Regional Clinical Research Associate
Job Code: CSA1013C
Northeast & Midwest – Spinal Device Study – 3 years monitoring, Device
a plus but not a must
Description
The primary responsibility of this position is to provide site management
and monitoring of clinical research studies. Responsibilities include site
monitoring, including verification of reported study data, investigational
product accountability, oversight of compliance and training of site staff
on regulatory and protocol-related issues, review of regulatory documents,
accurate and timely documentation, reporting, and communication, and
oversight of safety reporting. Average travel of 70% may be required.
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 monitor.
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, ability to
maintain an effective travel schedule, flexibility with changing priorities,
effective communication and personal skills necessary for successful
teamwork. General computer skills with proficiency in PC-based Microsoft
Word and Excel are mandatory.
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