Director, Clinical Science – Nephrology (Remote)

Travere Therapeutics

Atlanta (GA)

Remoto

USD 206.000 - 268.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Premium health insurance
Well-being programs
Retirement plan with employer match
Generous paid time off

Descrizione del lavoro

Travere Therapeutics seeks a Director of Clinical Science to lead nephrology development, guide trial design, and manage translational analyses. You will ensure GCP adherence while collaborating with cross-functional teams on INDs, NDAs, and BLAs, and contribute to regulatory submissions.

The role requires a PhD/PharmD/MD and 6+ years in pharma, with strong data interpretation, manuscript writing, and interaction with regulators and external partners.

Competenze

  • PhD, PharmD, and/or MD in Life Sciences is required; rare disease/nephrology experience preferred.
  • Experience in the pharmaceutical industry (6+ years) or equivalent.
  • Experience with clinical trials, INDs, NDAs, and BLAs is strongly preferred.

Mansioni

  • Assist in design and implementation of clinical studies and data analyses.
  • Assist in reporting clinical trial data for safety and efficacy.
  • Ensure Good Clinical Practices (GCPs) are followed.
  • Lead writing of clinical and data analysis reports and presentations.
  • Contribute to regulatory documents and sponsor communications.
  • Establish relationships with alliance partners and investigators.

Conoscenze

Organization
Presentation
Collaborative teamwork
Multidisciplinary work
Communication

Formazione

PhD/PharmD/MD in Life Sciences

Descrizione del lavoro

Travere Therapeutics seeks a Director of Clinical Science to lead nephrology development, guide trial design, and manage translational analyses. You will ensure GCP adherence while collaborating with cross-functional teams on INDs, NDAs, and BLAs, and contribute to regulatory submissions.

The role requires a PhD/PharmD/MD and 6+ years in pharma, with strong data interpretation, manuscript writing, and interaction with regulators and external partners.

Ottieni la revisione del curriculum gratis e riservata.

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