Clinical Lead (Lead Clinical Research Associate)

Avania; United States; On-site; USD 87,000 - 145,000; Full time

Benefits offered by this job

4 weeks PTO

Benefits

Job summary

Avania is hiring a Lead Clinical Research Associate to lead monitoring for medical device and MedTech studies in the United States. You will supervise project-specific monitoring activities, coordinate project-specific training, and act as the primary liaison for study questions from the monitoring team.

You will also drive peer review of required study documentation to ensure accuracy and quality, represent Avania on study calls, and support the Project Manager to ensure study objectives are

Job description

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.