Lead cardiovascular medical device studies in Marietta, Georgia, using clinical research expertise and knowledge of FDA regulations and ICH/GCP guidelines.

MiRus seeks a Clinical Trial Manager with at least two years of clinical research experience, preferably in cardiovascular medical devices. The position supports investigational studies from initiation through closure, collaborating with clinical, pre-clinical, research and development, data management, CRO, and site teams. You will contribute to protocols, regulatory documents, trial design, and study oversight.

Key Responsibilities:

- Manage investigational studies from start through study closure
- Write and edit protocols, consents, charters, and reports
- Oversee CRO and field study monitoring activities
- Monitor protocol compliance,



source documents, and case report forms
- Maintain trial master files, dashboards, trackers, and imaging

Requirements:

- Bachelor’s or Master’s degree in nursing
- Clinical cardiac experience in CCU, CVOR, or Cath Lab
- At least two years of clinical research experience
- Knowledge of FDA regulations and ICH/GCP guidelines
- Clinical trials experience in United States, Australia, or European Union

Apply cardiovascular clinical research expertise to protocols, compliance, monitoring, and study documentation at MiRus in Marietta.

📌 Cardiovascular Clinical Trial Manager (Montreal)
🏢 MiRus®
📍 Montreal