Strategic Director, Clinical Development (Rheumatology)

Meet Life Sciences Ltd.; New York (NY); On-site; USD 280,000 - 370,000; Full time

Job summary

Meet Life Sciences Ltd. in the United States is seeking a Senior Director of Clinical Development to shape clinical strategy for late-stage assets in rheumatology.

You will guide global programs, interact with regulatory bodies, and ensure safety monitoring while partnering with cross-functional teams on milestone achievement. The role is based on-site in the US, offering the opportunity to influence development plans, regulatory interactions, and strategic collaboration across global teams and

Qualifications

• Proven ability to design and lead early to late-stage clinical programs.
• Deep understanding of FDA, EMA, PMDA pathways and expectations.
• Leadership in matrixed, cross-functional settings with influence at all levels.
• Strong scientific judgment and analytical mindset.
• Excellent written and verbal communication with diverse stakeholders.
• Experience with combination drug‑device development is a plus.

Responsibilities

• Lead design, oversight, and interpretation of global Phase 1–2a programs with scientific rigor and regulatory compliance.
• Drive cross-functional planning for assets from discovery to development.
• Collaborate with in-licensing, acquisition, or collaboration teams on transition strategies.
• Monitor emerging science and evolving standards of care in relevant disease areas.
• Drive safety monitoring, benefit-risk assessments, and readiness for regulatory discussions.
• Influence global teams and external stakeholders through strategic communication.

Skills

Clinical program leadership

Global regulatory

Cross-functional leadership

Strategic thinking

Scientific communication

Combination therapy dev

Job description

Meet Life Sciences Ltd. in the United States is seeking a Senior Director of Clinical Development to shape clinical strategy for late-stage assets in rheumatology.

You will guide global programs, interact with regulatory bodies, and ensure safety monitoring while partnering with cross-functional teams on milestone achievement. The role is based on-site in the US, offering the opportunity to influence development plans, regulatory interactions, and strategic collaboration across global teams and