Senior Clinical Research PM - IDE Trials, Remote

CryoLife, Inc.; Kennesaw (GA); Remote; USD 120,000 - 180,000; Full time

Job summary

Artivion, Inc. is seeking a senior clinical studies professional to lead IDE programs and manage cross-functional teams across Regulatory, Quality, R&D, and Commercial.

The role focuses on advancing aortic repair technologies while ensuring compliance with protocols and regulatory requirements. You will oversee study sites, vendors, budgets, and timelines, develop clinical strategy, and contribute to abstracts, manuscripts, and presentations for scientific audiences.

Qualifications

• Bachelor’s degree required; Master’s preferred in a related field.
• 10+ years in clinical research or related field; IDE experience desirable.
• Experience with aortic repair technology or IDE studies desirable.
• Experience working at a medical device company desirable.
• Demonstrate project management, critical thinking, and communication skills.
• Proficient knowledge of medical terminology; willingness to travel.

Responsibilities

• Lead and manage all clinical studies for IDE programs with cross-functional teams.
• Oversee vendor management, budgets, timelines, and regulatory compliance.
• Develop clinical strategy and collaborate with Regulatory, Quality, R&D, and Commercial.
• Prepare study documents, reports, and regulatory submissions.
• Present at conferences and coordinate training and site support.

Skills

Project management

Critical thinking

Communication skills

Statistical analysis

Medical terminology

Travel readiness

Education

Bachelor’s degree

Master’s degree preferred

Job description

Artivion, Inc. is seeking a senior clinical studies professional to lead IDE programs and manage cross-functional teams across Regulatory, Quality, R&D, and Commercial.

The role focuses on advancing aortic repair technologies while ensuring compliance with protocols and regulatory requirements. You will oversee study sites, vendors, budgets, and timelines, develop clinical strategy, and contribute to abstracts, manuscripts, and presentations for scientific audiences.