Director, Clinical Development – Inflammation & Fibrosis

Gilead Sciences Inc.; Maryland; On-site; USD 261,000 - 338,000; Full time

Job summary

Gilead Sciences Inc. in the United States seeks a physician leader to drive multiple components of inflammation/fibrosis clinical programs, including PBC and MASH.

You will oversee study design, data analysis inputs, regulatory documentation, and scientific communications for late‑stage development. You will provide medical monitoring, cross‑functional guidance, and coordination of protocol design, study reports, and investigator presentations, with travel as needed.

Qualifications

• MD or equivalent with 4+ years' clinical, scientific and/or drug development experience in biopharma, healthcare, consulting, academia or related environment.
• Board certification in hepatology or gastroenterology preferred; other inflammatory backgrounds considered.
• Experience leading cross-functional project teams in life sciences or academia.
• Strong regulatory and medical monitoring expertise for clinical trials.

Responsibilities

• Leads development of Target Product Profiles and Clinical Development Plans for assigned molecules/products.
• Guides cross-functional teams to meet project deliverables and timelines.
• Contributes to protocol design, study reports, and health authority inquiries.
• Oversees medical monitoring and toxicity management in clinical trials.
• Coordinates data listings, summaries, and presentations of study results.
• Presents scientific information at conferences and investigator meetings.

Skills

MD/DO

Clinical development

Regulatory filings

Cross-functional leadership

Data analysis

Publications

Hepatology

Trial monitoring

Education

Board certification in hepatology/gastroenterology

Job description

Gilead Sciences Inc. in the United States seeks a physician leader to drive multiple components of inflammation/fibrosis clinical programs, including PBC and MASH.

You will oversee study design, data analysis inputs, regulatory documentation, and scientific communications for late‑stage development. You will provide medical monitoring, cross‑functional guidance, and coordination of protocol design, study reports, and investigator presentations, with travel as needed.