Rare Diseases Clinical Director - Phase 2 Regulation

george james ltd; United Kingdom; Hybrid; GBP 100,000 - 130,000; Part time

Benefits offered by this job

Equity/deferred payment during initial phase

Job summary

george james ltd is seeking an experienced Clinical Director for Rare Diseases. The role involves leading the finalisation and execution of a Phase 2 clinical program and requires an MD/PhD with Phase 2 clinical development experience.

Strong regulatory insight (FDA/EMA) is essential, and experience in rare diseases is desirable. The role is initially part-time with potential to move to a full-time position post-funding.

Qualifications

• Experience in Phase 2 clinical development is essential.
• Strong regulatory insight from FDA/EMA is required.
• Experience in rare diseases is desirable.

Responsibilities

• Finalise Phase 2 protocol, endpoints, and regulatory strategy.
• Align clinical documentation to investor- and regulator-ready standard.
• Lead CRO selection and trial readiness.

Skills

Regulatory insight (FDA/EMA)

Phase 2 clinical development

Leadership

Detail-oriented

Education

MD/PhD

Job description

george james ltd is seeking an experienced Clinical Director for Rare Diseases. The role involves leading the finalisation and execution of a Phase 2 clinical program and requires an MD/PhD with Phase 2 clinical development experience.

Strong regulatory insight (FDA/EMA) is essential, and experience in rare diseases is desirable. The role is initially part-time with potential to move to a full-time position post-funding.