Clinical Research Monitor - Remote

Overview

As a Clinical Research Monitor at Edwards Lifesciences, you will play a crucial role in ensuring the safety and compliance of clinical trials that impact patient outcomes, particularly in the field of cardiovascular health.

In Short

• Field monitoring of clinical trials to ensure patient safety.
• Assure trials are conducted ethically and within regulatory compliance.
• Develop and deliver training on GCPs and protocols.
• Provide oversight and insights into trial activities.
• Contribute to the development of clinical protocols and consent forms.
• Track investigational device accountability.
• Verify trial data and maintain regulatory documents.
• Edit informed consent documents as needed.
• Act as a mentor to junior employees.
• Travel up to 75% for clinical site visits.

Requirements

• Bachelor's Degree in Life Sciences or Nursing.
• 3 years of experience in clinical research or related fields.
• Experience in medical device or regulated industry.
• Strong communication and analytical skills.
• Experience with electronic data capture.
• Understanding of cardiovascular anatomy and physiology.
• Proficiency in MS Office Suite and clinical systems.
• Problem-solving and critical thinking skills.
• Technical writing skills.
• COVID-19 vaccination required.

Benefits

• Competitive salaries and performance-based incentives.
• Wide variety of benefits programs.
• Opportunities for professional growth.
• Supportive work environment focused on patient care.
• Mentorship and training programs.