Remote MD Clinical Development Lead – Pulmonary

Pulmovant; United States; Remote; USD 210,000 - 330,000; Full time

Job summary

Pulmovant seeks a highly motivated hands-on physician leader who will be responsible for the design and execution of clinical trial activities to support the development of mosliciguat, including study design, protocol development, execution and data interpretation.

The candidate will be the primary medical lead, liaising between investigators and the internal study team, maintaining relationships with key opinion leaders and Health Authorities, and leading the Phase 3 trial along with potential

Qualifications

• MD/DO degree or equivalent is required.
• Board Certification or Board Eligibility in internal medicine with subspecialty training or experience in drug development is desirable.
• Minimum of 5–7 years experience conducting clinical trials in biopharma, preferably late phase.

Responsibilities

• Provide clinical and scientific input to study design, protocol concepts and development, statistical analysis plans and reporting.
• Medical oversight for study designs, protocol development, and regulatory documents in collaboration with cross-functional teams.
• Lead trial execution and management of clinical studies with focus on the Phase 3 trial, including recruitment, site activation, data review and reporting.
• Stay current on therapeutic landscape and regulatory issues to guide program direction.
• Collaborate with investigators, internal teams, and external experts to ensure appropriate study designs and outcomes.
• Maintain knowledge of ICH-GCP, external regulations and procedures.

Skills

MD/DO degree

Clinical trial leadership

Study design

Regulatory knowledge

Cross-functional collaboration

GCP compliance

Travel willingness

Education

MD/DO degree or equivalent

Job description

Pulmovant seeks a highly motivated hands-on physician leader who will be responsible for the design and execution of clinical trial activities to support the development of mosliciguat, including study design, protocol development, execution and data interpretation.

The candidate will be the primary medical lead, liaising between investigators and the internal study team, maintaining relationships with key opinion leaders and Health Authorities, and leading the Phase 3 trial along with potential