About this role
Role Overview
- Leading the activities involved in the management of clinical research studies
- Managing clinical trial sites, including monitoring and/or overseeing assigned clinical research associates
- Supporting product development teams by collecting clinical trial evidence
- Communicating study results through presentations at technical meetings
- Developing a knowledge and understanding of assigned products, customers, customer needs
Requirements
- Bachelor’s Degree or higher
- 5 years of recent clinical research-related study project manager and/or monitoring experience
- Clinical research certification (SOCRA or ACRP)
- Knowledge of Good Clinical Practice guidelines and regulations
- Advanced capabilities in E-mail, Word, Excel, PowerPoint and Windows applications
- Current, valid driver’s license is desired.
Benefits
- Medical, Dental & Vision
- Health Savings Accounts
- Health Care & Dependent Care Flexible Spending Accounts
- Disability Benefits
- Life Insurance
- Voluntary Benefits
- Paid Absences
- Retirement Benefits