Role OverviewPerform site monitoring visits, adapt and drive subject recruitment plans, and manage study site practices to ensure compliance with study protocols, regulations, and sponsor requirements. Work with sites to establish regular lines of communication and manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices and escalate quality issues as necessary.
What You Will Do
Perform site monitoring visits, work with sites to adapt and drive subject recruitment plans, manage study site practices, and evaluate the quality and integrity of study site practices. Collaborate with study team members and support project execution as necessary.
Why It Might Be a Fit
This role requires a strong understanding of clinical research regulatory requirements, good therapeutic and protocol knowledge, and effective communication and problem-solving skills. The ideal candidate will have at least 2 years of on-site monitoring experience and a strong command of the English language.
Requirements
- Bachelor's Degree in scientific discipline or healthcare preferred
- At least 2 years of on-site monitoring experience
- Good knowledge of and skill in applying applicable 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
- Potential base pay range of $57,500.00 - $226,800.00
- Incentive plans, bonuses, and/or other forms of compensation
- Range of health and welfare benefits
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