Senior Clinical Research Monitor – Cardio Trials

Edwards Lifesciences; Phoenix (AZ); On-site; USD 108,000 - 153,000; Full time

Job summary

Edwards Lifesciences in Phoenix, AZ, is seeking a field-monitoring professional to join our Clinical Affairs team. You will monitor clinical trials, ensure data integrity, and verify regulatory documentation to support evidence for safe, effective devices.

Responsibilities include training on GCPs, mentoring junior staff, validating device accountability, contributing to protocol development, and communicating with investigators and study sponsors. Domestic travel up to 75% is required.

Qualifications

• Excellent written and verbal communication skills.
• Strong presentation and interpersonal abilities.
• Analytical thinking and problem-solving capabilities.
• Experience with regulatory compliance and quality systems.

Responsibilities

• Field monitoring of studies and data collection for clinical trials.
• Developing and delivering training on GCPs, protocols, and regulatory requirements.
• Mentoring new or junior employees and overseeing trial activities.
• Providing insights into protocol compliance, enrollment, and data quality.
• Contributing to protocol development, informed consent forms, and CRFs.
• Validating investigational device accountability and source documentation.
• Verifying trial data and regulatory documents through audits.
• Editing or amending informed consent documents.

Skills

Communication skills

Presentation skills

Interpersonal skills

Analytical skills

Education

Bachelor's degree or equivalent in related field

Tools

MS Office

Word

Excel

Adobe

Job description

Edwards Lifesciences in Phoenix, AZ, is seeking a field-monitoring professional to join our Clinical Affairs team. You will monitor clinical trials, ensure data integrity, and verify regulatory documentation to support evidence for safe, effective devices.

Responsibilities include training on GCPs, mentoring junior staff, validating device accountability, contributing to protocol development, and communicating with investigators and study sponsors. Domestic travel up to 75% is required.