Clinical Research Associate II - Remote

Overview

The CRA II assists in the execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products, working with confidential patient and company data.

In Short

• Serve as site manager ensuring timely data entry and query resolution.
• Participate in monitoring functions including site management and compliance checks.
• Conduct training at investigational sites as needed.
• Manage device accountability and regulatory documentation.
• Conduct site visits and act as a liaison to resolve issues.
• Assist in developing and distributing study-related documents.
• Provide mentoring to junior staff.
• Maintain project timelines and prepare routine reports.
• Adhere to quality management systems and regulations.
• Perform other duties as assigned.

Requirements

• Bachelor's degree in biological sciences or health-related field.
• 3+ years of experience in clinical/scientific research or medical devices.
• 1+ years of clinical monitoring experience preferred.
• Knowledge of medical terminology and clinical study regulations.
• Excellent communication and organizational skills.
• Intermediate proficiency in Microsoft Office.
• Ability to work on multiple projects and provide guidance.

Benefits

• Competitive compensation package.
• Benefits and equity program when applicable.
• Individual total compensation varies based on qualifications and location.