Senior Director, Clinical Science — Nephrology (Remote)

Travere Therapeutics; Washington (District of Columbia); Remote; USD 206,000 - 268,000; Full time

Benefits offered by this job

Premium health benefits

Well-being programs

Retirement plan with employer match

Generous paid time off

Job summary

Travere Therapeutics in San Diego invites a Director, Clinical Science to lead nephrology development across programs. You will collaborate with cross-functional teams on trial design, data analyses, and regulatory readiness, ensuring GCPs are followed and data are presented clearly.

Requirements include a PhD, PharmD, or MD in life sciences, 6+ years in pharma, and experience with INDs/NDAs/BLAs. You will write clinical reports, contribute to regulatory submissions, build external partnerships,

Qualifications

• PhD, PharmD or MD in life sciences with relevant rare disease nephrology experience.
• 6+ years in the pharmaceutical industry or equivalent experience in academia or industry.
• Experience with INDs, NDAs, BLAs and regulatory information requests preferred.

Responsibilities

• Design and implement clinical studies and data analyses.
• Report clinical trial data for safety and efficacy with team collaboration.
• Ensure GCP compliance across studies and data handling.
• Lead writing of clinical and data analysis reports and regulatory documents.
• Build and maintain external alliances to optimize collaborations.
• Prepare manuscripts and present findings at scientific meetings.

Skills

Clinical trial design

Data analysis

GCP compliance

Regulatory submissions

Cross-functional leadership

Presentation skills

Education

PhD, PharmD, or MD in Life Sciences

6+ years pharma industry experience

Job description

Travere Therapeutics in San Diego invites a Director, Clinical Science to lead nephrology development across programs. You will collaborate with cross-functional teams on trial design, data analyses, and regulatory readiness, ensuring GCPs are followed and data are presented clearly.

Requirements include a PhD, PharmD, or MD in life sciences, 6+ years in pharma, and experience with INDs/NDAs/BLAs. You will write clinical reports, contribute to regulatory submissions, build external partnerships,