Sr. Clinical Research Associate (Cardiac Catheter Products)

About the Role

As the Sr. Clinical Research Associate (Sr. CRA) you’ll be responsible for managing and monitoring activities that will lead to successful execution of clinical studies at US and international clinical sites. You will monitor patient recruitment, data and study related information related to clinical sites and study participation. Ensure that duties are performed in accordance with the Code of Federal Regulations (CFR) of the Food and Drug Administration (FDA) and the International Conference on Harmonization - Good Clinical Practice (ICH-GCP).

To Make an Impact, You Will:

• Provide case support to research sites across multiple studies with minimal guidance.
• Prepare and develop project and study-related documents including informed consent forms, CRFs, study guides, study reference binders, and patient diaries.
• Coordinate review of data listings and preparation of interim and final clinical study reports.
• Be responsible for monitoring clinical studies.