Role OverviewPerform site monitoring visits, adapt and drive subject recruitment plans, administer protocol and related study training, evaluate site quality and integrity, and manage study progress. Work with sites to ensure compliance with study protocol, regulations, and sponsor requirements.
What You Will Do
Perform site monitoring visits, adapt and drive subject recruitment plans, administer protocol and related study training, evaluate site quality and integrity, 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 strong organizational and problem-solving skills.
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 therapeutic and protocol knowledge
- computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
- written and verbal communication skills
- organizational and problem-solving skills
- effective time and financial management skills
Benefits
- health and welfare benefits
- incentive plans, bonuses, and/or other forms of compensation
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