Role OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
What You Will Do
Perform site monitoring visits, work with sites to adapt and track subject recruitment plan, administer protocol and related study training, evaluate study site practices, and manage study progress.
Why It Might Be a Fit
Requires at least 2 years of on-site monitoring experience, good knowledge of clinical research regulatory requirements, and good therapeutic and protocol knowledge.
Requirements
- Bachelor's Degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of clinical research regulatory requirements
- Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Benefits
- Health and welfare benefits
- Incentive plans, bonuses, and/or other forms of compensation
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