Senior Clinical Scientist - Rare Disease Trials (Remote)

Travere Therapeutics; Denver (CO); Remote; USD 150,000 - 195,000; Full time

Job summary

Travere Therapeutics seeks an Associate Director of Clinical Science to support ongoing and future clinical development. You will collaborate with cross-functional study teams on trial design, data analyses, and regulatory documentation, ensuring adherence to GCP.

The role requires advanced scientific training and 4+ years in pharma, with experience in rare disease and IND/ NDA submissions, plus ability to travel up to 15%. This position is based in San Diego with some remote flexibility.

Qualifications

• PhD, PharmD, or MD in a related life science discipline required. Equivalent combination of education and applicable job experience may be considered.
• 4+ years of relevant experience in the pharmaceutical industry required; experience in rare disease preferred.
• Experience supporting clinical trials and clinical studies required; experience with human pharmacology studies preferred.

Responsibilities

• Lead clinical science components of assigned study plans and contribute to protocol design and implementation.
• Review, interpret, summarize clinical trial safety and efficacy data; identify findings and questions for discussion with the clinical development team.
• Coordinate assigned clinical science activities, timelines, and deliverables across study teams, maintaining accurate and well-organized documentation.
• Support study conduct in accordance with protocols, applicable regulations, and Good Clinical Practice (GCP).
• Lead the preparation and scientific review of clinical and data analysis reports, slide presentations, and ClinicalTrials.gov summaries in collaboration with internal and external partners.
• Contribute clinical, scientific, and mechanism-of-action content to INDs, NDAs, BLAs, and related submissions, including protocols, statistical analysis plans, mock tables, figures, and listings, investigator brochures, medical reports, efficacy and safety summaries, scientific rationales, benefit-risk assessments, regulatory briefing books, and responses to regulator requests.
• Build and maintain productive working relationships and represent the clinical science team with alliance partners, external companies, investigators, and key opinion leaders.
• Contribute to manuscripts for scientific and medical journals and to presentations at scientific meetings.
• Additional duties assigned as needed.

Skills

Cross-functional collaboration

Data interpretation & presentation

Scientific writing

Attention to detail

Education

PhD/PharmD/MD in life sciences

Job description

Travere Therapeutics seeks an Associate Director of Clinical Science to support ongoing and future clinical development. You will collaborate with cross-functional study teams on trial design, data analyses, and regulatory documentation, ensuring adherence to GCP.

The role requires advanced scientific training and 4+ years in pharma, with experience in rare disease and IND/ NDA submissions, plus ability to travel up to 15%. This position is based in San Diego with some remote flexibility.