Opportunity for a experienced Clinical Research Associate with experience in medical device trails to join a well respected and well known sponsor organization. This role is ideal for a hands-on professional with strong technical expertise and a proven ability to independently manage high-performing sites.

Location: Remote (U.S., Midwest/Central or East Coast preferred)
Contract: 12-Month Renewable
Compensation: $65-80/hr (DOE)
Travel: ~60% (≈2 weeks/month)

We are seeking an experienced Senior or Principal CRA to support complex Medical Device clinical trials. 

Key Responsibilities

• Conduct monitoring visits (PSV, SIV, RM, COV) across East Coast and Midwest sites
• Oversee site performance, enrollment, and long-term patient follow-up
• Ensure compliance with study protocols, IDE regulations, and ISO 14155 standards
• Maintain strong relationships with investigators and site teams

Qualifications

• 5+ years CRA experience at Senior or Principal level
• Direct Medical Device trial monitoring experience required
• Cardiology experience strongly preferred
• Strong site management and data integrity focus
• Ability to travel ~60%
• Must be U.S.-based (Central Time Zone preferred)

#LI-ZW1
​​​​​​​