Senior Medical Director

Discover an exciting leadership opportunity within a pioneering biotechnology firm dedicated to developing innovative cardiovascular therapies. If you're passionate about advancing medical science and shaping the future of cardiovascular health, this role offers a chance to make a meaningful impact while working alongside a dynamic global team.

Our client is a clinical-stage biotech company focused on creating first- and best-in-class therapies for cardiovascular and metabolic conditions. With ongoing multi-regional clinical trials and preparations for a major market introduction, the company is seeking a Senior Medical Director to lead strategic clinical efforts in the US.

In this role, you will be the key medical authority for the company’s cardiovascular programs in the US, contributing to the design, execution, and oversight of pivotal clinical trials. You will collaborate with global teams and interface with investigators, key opinion leaders, and regulatory bodies, ensuring the scientific integrity and regulatory compliance of all clinical activities. Your insights and leadership will directly influence the success and progression of transformative therapies in development.

Key Responsibilities:

• Lead the development and execution of US medical strategy aligned with the company’s global clinical plans.
• Design clinical trial protocols, ensuring scientific rigor and regulatory compliance.
• Oversee trial execution as a primary medical monitor, interpreting data and addressing clinical queries.
• Represent the company in interactions with US regulatory authorities and contribute to submissions.
• Build and maintain relationships with US-based KOLs, investigators, and academic institutions.
• Support scientific communication efforts through conference presentations and publications.
• Collaborate seamlessly with global teams to drive continuous progress in clinical development.

What You Need to Succeed:

• M.D. degree with board certification or equivalent in Cardiology, Cardiovascular Diseases, or Internal Medicine (preferred).
• Over 8 years of experience in clinical development within the biopharmaceutical or CRO industry, especially in cardiovascular or related fields.
• Proven expertise in late-phase (Phase II/III) clinical trials and experience interacting with US FDA.
• Strong understanding of US regulations, ICH/GCP standards, and drug development processes.
• Excellent leadership, communication, and strategic thinking skills, with the ability to operate independently in a fast-paced, cross-cultural environment.