Senior CRA - Medical Device JB-3486

Our company is seeking a diligent and experienced Clinical Research Associate to join our team as an external consultant. The CRA will monitor clinical studies across various university sites, ensuring the integrity of data and compliance with regulatory requirements.

Key Responsibilities:

• Site Monitoring: Travel between university sites to monitor clinical studies, ensuring adherence to protocols and regulatory guidelines.
• Patient Enrollment: Hands-on involvement in the recruitment and enrollment of patients.
• Data Collection and Analysis: Collect, manage, and analyze clinical data to ensure accuracy and completeness.
• Collaboration: Work closely with our back office team, faculty members, and other stakeholders to facilitate smooth study operations.
• Communication: Maintain clear and consistent communication with all parties involved in the clinical studies.
• Compliance: Ensure all activities are conducted in accordance with regulatory standards and company policies.

Requirements:

• Bachelor’s degree in a relevant field - a must, advanced degree - an advantage.
• Proven experience as a Clinical Research Associate - a must.
• In-depth knowledge of clinical trial processes and regulations in the medical device field- a must.
• Previous dental studies - big advantage.
• Strong analytical and organizational skills.
• Excellent communication and interpersonal abilities.
• Ability to travel frequently between sites (USA) - a must.