Clinical Lead (Lead Clinical Research Associate)

Our take on this role

About this role

Supervise monitoring activities for medical device and MedTech studies, coordinate study-team training, and review study documentation. The position requires travel approximately 25–30% of the time.

What could you bring from clinical work?

• Nurses and SLPs: Checking clinical documentation for accuracy and completeness could help you review required study documentation.
• OTs: Your experience teaching colleagues clinical procedures and checking implementation may help with coordinating project-specific training.
• PTs: Experience reviewing clinical documentation for adherence to evidence-based procedures could help you review monitoring reports.

Full job description from Avania

Avania is hiring - 3 x Clinical Lead (Lead Clinical Research Associate)

Salary Up to $145,000 + 10% bonus potential - 4 weeks PTO + Benefits

As Clinical Trials Lead (Lead Clinical Research Associate), you will work with a sponsoring company in the monitoring of medical device and MedTech studies with an emphasis placed on ensuring the highest ethical and clinical standards.

You will also assume a key role in the monitoring team by supervising project-specific monitoring activities, coordinating project-specific training, and interacting with our clients. Avania's Lead Clinical Research Associate (CTL / Lead CRA) acts as the primary contact for study questions from the monitoring team, organizes team training and study updates, and generates necessary monitoring tools. You will ensure monitoring visits are being conducted as needed and tasks are being completed in an appropriate and timely manner. Further, you will complete peer review of required study documentation to ensure these are accurate, complete, and of high quality. You will also represent Avania on study conference calls and/or meetings.

The Lead CRA will collaborate with the Project Manager to ensure study objectives are met. You may also handle CRA study activities as needed. Finally, you will provide CRA support, including such activities as assisting Clinical Research Associates with difficult or challenging situations or corrective actions, conducting co-visits and providing feedback, reviewing monitoring reports, and similar work.

This position requires travel approximately 25 – 30% of the time.