Director, Medical Affairs - Electrophysiology

Johnson & Johnson Co.; Irvine (CA); Sur place; USD 164 000 - 306 000; Plein temps

Avantages offerts par ce poste

Competitive compensation

401k

Medical insurance

Dental insurance

Vision insurance

Exercise reimbursement

Flexible time off

Paid parental leave

Volunteer leave

Résumé du poste

Johnson & Johnson in Irvine, CA is seeking a Director of Medical Affairs, Electrophysiology to lead clinically driven strategy and evidence generation for electrophysiology devices. You will partner with R&D, Regulatory, Quality and Marketing to shape product development, clinical studies, and lifecycle management.

You will build external relationships with key opinion leaders, surgeons, and regulatory bodies, oversee study design and execution, ensure safety and compliance, and drive training

Qualifications

• Bachelor's degree in Medicine or related life sciences.
• MD/PhD or PharmD highly preferred.
• Minimum 10 years of experience in product development within the cardiovascular field.

Responsabilités

• Lead regulatory and commercial strategy support for product development and lifecycle management.
• Oversee clinical studies, data analysis, and publication support for regulatory submissions.
• Provide medical insights to Marketing, R&D, Regulatory, and Quality teams across global launches.
• Engage external stakeholders including Key Opinion Leaders, surgeons, and regulatory agencies.
• Ensure adherence to safety, ethics, and compliance in all Medical Affairs activities.

Connaissances

Strategic leadership

Clinical & scientific expertise

Regulatory awareness

Stakeholder management

Medical affairs experience

Cardiovascular knowledge

Formation

Bachelor's degree in Medicine, Biomedical/Mechanical Engineering or related life sciences

MD/PhD/PharmD highly preferred

Description du poste

Johnson & Johnson in Irvine, CA is seeking a Director of Medical Affairs, Electrophysiology to lead clinically driven strategy and evidence generation for electrophysiology devices. You will partner with R&D, Regulatory, Quality and Marketing to shape product development, clinical studies, and lifecycle management.

You will build external relationships with key opinion leaders, surgeons, and regulatory bodies, oversee study design and execution, ensure safety and compliance, and drive training