Senior Director, Clinical Development — Pulmonary PH-ILD

OpenKrill; United States; Remote; USD 180,000 - 240,000; Full time

Job summary

Pulmovant is seeking a highly motivated hands-on physician leader who will be responsible for the design and execution of clinical trial activities to support mosliciguat development, including study design, protocol development, execution and data interpretation. The candidate will be the primary source of medical accountability and oversight for clinical trials and will serve as a medical lead.

The role includes leading the Phase 3 trial and may include indication lead activities for

Qualifications

• MD/DO degree is required.
• Board Certification or Board Eligibility in internal medicine with subspecialty training or experience in drug development in cardiopulmonary/respiratory medicine is desirable.
• Minimum 5–7 years of experience conducting clinical research trials in biopharmaceutical industry, ideally late phase.
• Hands-on experience in protocol development and clinical trial monitoring.
• Experience with US and European Health Authority interactions and submission of regulatory documents is desirable.
• Strong written and verbal communication skills; ability to lead cross-functional teams.

Responsibilities

• Provide clinical leadership for Phase 3 trial design and execution.
• Medical accountability and oversight for trials; liaise between investigators and internal study team.
• Prepare and contribute to regulatory documents, safety reports, and study reports.
• Present at investigator meetings and liaise with Health Authorities.
• Mentor internal and external colleagues and collaborate across functions.

Skills

Clinical trial leadership

Protocol development

Regulatory submissions

Cross-functional collaboration

Medical oversight

Health Authority interactions

Education

MD/DO

Job description

Pulmovant is seeking a highly motivated hands-on physician leader who will be responsible for the design and execution of clinical trial activities to support mosliciguat development, including study design, protocol development, execution and data interpretation. The candidate will be the primary source of medical accountability and oversight for clinical trials and will serve as a medical lead.

The role includes leading the Phase 3 trial and may include indication lead activities for