Senior Clinical Science Lead - Rare Disease (Remote)

Travere Therapeutics Inc.; San Diego (CA); Hybrid; USD 150,000 - 195,000; Full time

Benefits offered by this job

Premium health

Retirement plans with employer match

Life insurance

Disability insurance

Generous paid time off

Wellness programs

Job summary

Travere Therapeutics, Inc. is seeking an Associate Director, Clinical Science to advance ongoing and future clinical development and lifecycle activities.

You will work with cross-functional study teams on trial design, data analyses, and results interpretation, ensuring studies comply with GCP and regulatory standards. The role requires 4+ years in pharma, a PhD/MD/PharmD, and strong collaboration with internal and external partners to deliver translational science supporting INDs and

Qualifications

• PhD, PharmD, or MD in a related life science discipline required.
• 4+ years of relevant experience in the pharmaceutical industry required; rare disease preferred.
• Experience supporting clinical trials and clinical studies required; human pharmacology experience preferred.

Responsibilities

• Lead clinical science components of assigned study plans and protocol design.
• Review and summarize clinical trial safety/efficacy data.
• Coordinate clinical science activities, timelines, and deliverables across study teams.
• Support study conduct per protocols and regulatory requirements (GCP).
• Prepare and review clinical and data analysis reports and regulatory submissions.
• Contribute to INDs/NDAs/BLAs and related regulatory documents.
• Foster relationships with alliance partners and key opinion leaders.
• Contribute to manuscripts and scientific presentations.

Skills

Cross-functional collaboration

Scientific communication

Attention to detail

Education

PhD/PharmD/MD in life sciences

4+ years pharma industry

Tools

IND/NDAs/BLAs

GCP compliance

Job description

Travere Therapeutics, Inc. is seeking an Associate Director, Clinical Science to advance ongoing and future clinical development and lifecycle activities.

You will work with cross-functional study teams on trial design, data analyses, and results interpretation, ensuring studies comply with GCP and regulatory standards. The role requires 4+ years in pharma, a PhD/MD/PharmD, and strong collaboration with internal and external partners to deliver translational science supporting INDs and