Clinical Research Associate (I and/or II)

Cleveland, OH       ·       Full time

Location: Cleveland, OH

Responsibilities:

• Coordinates and implements clinical study activities for product development projects. 
• Works directly with the clinical, research, and regulatory staff to execute clinical studies.
• Trains clinical site staff on study protocols, use of devices according to the Instructions for Use, and Good Clinical Practices.
• Coordinates and monitors clinical studies to ensure subject safety, compliance with study protocols, regulatory requirements, and Good Clinical Practices.

Requirements:

• BS degree or higher in Life Sciences or related technical or clinical field.
• 1-2 years related research and monitoring experience preferred, preferably in the Medical Device industry. 
• Experience with the design, management and conduct of medical device or drug related clinical studies.
• Knowledge of FDA guidelines and Good Clinical Practices.
• Ability to travel up to 20% for CRA I and up to 40% for CRA II
• Ability to handle several priorities within the clinical research process.
• Ability to reason independently and recommend specific solutions in clinical settings.
• Ability to work independently, prioritize, and work within a team environment.

Why Join Our Team?

• Voted Top Workplace in 2022
• Competitive salary with company-paid medical, dental, and vision benefits
• High growth company with game changing technology
• A passion for improving the lives of millions of pain sufferers
• Flexible work/life balance

Please click here to learn more.