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Description:
The leading niche is seeking qualified clinical research associates to perform site monitoring visits at clinical centers conducting u.sGovernment and commercial-sponsored research in multiple therapeutic areasExperience study coordinators will be considered for this positionOpenings are available in a regional home-based office.
Requirements:
Job responsibilities: assist with development of site monitoring plans, conduct site initiation visits, interim visits, and close-out visits of multiple therapeutic areas assessing compliance with the research protocol, ich/gcp, fda, and other applicable regulations, and write detailed reports of findingsSupport site compliance with good clinical practice (gcp) including site training, performance improvement recommendations, and corrective and preventive action plans (capa)Contribute to site training, risk assessment, and quality assurance practices.
Basic qualifications: a bachelor’s degree, preferably in nursing or other health-related field and clinical research experience is required.
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Posted 30+ days ago
