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. The role involves site monitoring visits, adapting and driving subject recruitment plans, administering protocol and related study training, evaluating study site practices, and managing study progress.
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 by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution.
Why It Might Be a Fit
To be eligible for this position, you must reside in the same country where the job is located. The role requires at least 2 years of on-site monitoring experience, good knowledge of and skill in applying applicable clinical research regulatory requirements, and good therapeutic and protocol knowledge.
Requirements
- Bachelor's Degree in scientific discipline or health care 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 as provided in company training
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
- Written and verbal communication skills including good command of English language
- Organizational and problem-solving skills
- Effective time and financial management skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
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 and/or other benefits
]]>