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 drive subject recruitment plans, administer protocol and related study training, evaluate study site practices, and manage study progress.
Why It Might Be a Fit
Requires strong knowledge of clinical research regulatory requirements, therapeutic and protocol knowledge, and effective communication 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
]]>