Director, Clinical Science – Rare Diseases (Remote)

Travere Therapeutics; Columbus (OH); Hybrid; USD 150,000 - 195,000; Full time

Job summary

Travere Therapeutics seeks an Associate Director, Clinical Science to support ongoing and future clinical development and lifecycle activities. You will work with cross-functional teams to design trials, analyze translational and clinical data, and present results, ensuring studies follow GCP.

The role involves coordinating deliverables, contributing to INDs/NDAs/BLAs, and collaborating with alliance partners and investigators across development stages.

Qualifications

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

Responsibilities

• Lead clinical science components of assigned study plans and contribute to protocol design and implementation.
• Review and interpret clinical trial safety and efficacy data; identify questions for discussion with the team.
• Coordinate activities, timelines, and deliverables across study teams with well-organized documentation.
• Support study conduct in accordance with protocols and GCP.
• Lead preparation and scientific review of reports, presentations, and ClinicalTrials.gov summaries in collaboration with partners.
• Contribute to INDs, NDAs, BLAs, and regulatory information requests with protocols, SAPs, figures, and listings.
• Build relationships with alliance partners, investigators, and KOLs to support activities and collaborations.
• Contribute to manuscripts and scientific presentations.

Skills

Clinical science

Data analysis

Cross-functional teamwork

Regulatory submissions

IND/NDAs/BLAs

Education

PhD/MD/PharmD

Job description

Travere Therapeutics seeks an Associate Director, Clinical Science to support ongoing and future clinical development and lifecycle activities. You will work with cross-functional teams to design trials, analyze translational and clinical data, and present results, ensuring studies follow GCP.

The role involves coordinating deliverables, contributing to INDs/NDAs/BLAs, and collaborating with alliance partners and investigators across development stages.