Clinical Lead (Lead Clinical Research Associate)

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

Benefits offered by this job

Bonus potential

4 weeks PTO

Benefits

Job summary

Avania is hiring for Lead Clinical Research Associate to monitor medical device and MedTech studies with an emphasis on ethical and clinical standards. You will supervise monitoring activities, coordinate project-specific training, and serve as primary contact for study questions.

You will perform peer reviews of study documentation, represent Avania in conference calls, and collaborate with the Project Manager to meet study objectives. Travel approximately 25–30% of the time is required.

Qualifications

• Experience monitoring medical device/MedTech trials.
• Must supervise monitoring activities and training.
• Willingness to travel 25–30% of time.

Responsibilities

• Supervise project-specific monitoring activities and ensure timely completion.
• Coordinate project-specific training and study updates.
• Act as primary contact for study questions from the monitoring team and clients.
• Peer review of required study documentation for accuracy and quality.
• Represent Avania on study calls/meetings and collaborate with PM to meet objectives.

Skills

Clinical monitoring

Team leadership

Training coordination

Regulatory compliance

Education

Bachelor's degree in life sciences

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.