Description

In this role, you will shape the cardiovascular outcomes strategy while collaborating with cross-functional teams. Your expertise will guide clinical development, mentor peers, and ensure successful treatment progression through regulatory processes.

Requirements

• •Extensive experience in late stage drug development
• •MD (board certified in Cardiology preferred)
• •Significant clinical trial experience in CVRM studies
• •Minimum 5 years of pharma/biotech R&D experience
• •Experience authoring global trial plans
• •Championing novel approaches to clinical development
• •Strong external network with relevant experts for CVOTs
• •Regulatory experience for submissions and processes
• •Ability to collaborate with internal and external partners
• •Strong interpersonal, verbal, and written communication skills
• •Experience in Heart Failure Clinical Programs

Tasks

• •Guide cardiovascular outcomes strategy
• •Collaborate with clinical research teams
• •Work with regulatory affairs and medical affairs
• •Ensure successful treatment progression
• •Understand cardiovascular diseases and clinical trial protocols
• •Interact with regulatory agencies for study standards
• •Provide insights for project development and effectiveness
• •Mentor physicians and scientists in disease expertise
• •Author global trial plans
• •Run large cardiovascular outcome trials
• •Champion innovative clinical development approaches
• •Provide clinical science input for regulatory submissions
• •Collaborate with internal and external partners
• •Build relationships with clinical investigators and KOLs
• •Influence internal partners and stakeholders