Clinical Project Manager

Opportunity to join a small medical devices company in the urology space that have 3 ongoing clinical trials. The Clinical Project Manager will ensure that clinical trials are executed on time, within budget, and in compliance with regulatory standards to support product development and commercialization goals.

Key Responsibilities:

• Manage and execute clinical studies, including feasibility, pivotal, and post-market studies, for urology medical devices.
• Coordinate site selection, study initiation, monitoring, and close-out activities.
• Ensure adherence to regulatory requirements (e.g., FDA, MDR) and Good Clinical Practice
• Identify and mitigate project risks, ensuring timely resolution of issues.
• Manage Contract Research Organizations (CROs), vendors, and clinical sites, ensuring high-quality deliverables.

Qualifications and Experience:

• Bachelor’s degree in life sciences, nursing, or a related field; advanced degree preferred.
• Minimum 5 years of clinical research experience in the medical device industry, with at least 2 years in a project management role.
• Proven experience managing clinical studies in the urology therapeutic area is desirable but not required.
• Remote role, ideally based on the East Coast