Job Description

Clinical Research Associate

Step into a role where your work directly supports groundbreaking therapies that can transform the lives of heart‑failure patients worldwide. In this position, you’ll be an essential force behind clinical studies that bring life‑changing medical innovations to the people who need them most. Join my client and help advance science with purpose and impact.

Why You Should Apply

• Be part of a mission-driven organization advancing novel cardiac therapies
• Work cross‑functionally with clinical, regulatory, commercial, and global teams
• Opportunity to support high‑visibility clinical studies in an innovative environment
• Competitive benefits package (medical, retirement, etc.)

What You’ll Be Doing

• Manage and organize administrative aspects of assigned clinical trials
• Support monitoring visit scheduling and report review
• Prepare meeting minutes and maintain study documentation
• Train site staff and assist as a resource for monitors and clinical sites
• Track regulatory documents, collect outstanding records, and oversee IRB renewal notifications
• Maintain and audit study files, support resolution of monitoring findings
• Coordinate testing with Core Labs and ensure compliance with SOPs
• Arrange key clinical meetings and assist in preparation
• Review and approve Site Qualification Reports
• Train users on EDC, eBinders, and related systems
• Manage CTMS data for budgets, site payments, and invoice processing

About You

• Be able to do the job as described.
• Experience using IBM EDC, ClinPlus CTMS, Florence e‑Binders, Egnyte, or similar tools
• Familiarity with FDA regulations and GCP
• Experience interacting with hospital administrators and research coordinators
• Background in medical device or heart‑failure clinical trials
• Bachelor’s degree in life sciences or related field preferred or equivalent work experience.

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