Senior Clinical Scientist, Rare Disease (Remote)

Travere Therapeutics; Wichita (KS); Remote; USD 150.000 - 195.000; Vollzeit

Benefits dieser Stelle

Premium health benefits

Retirement plan with employer match

Generous paid time off

Zusammenfassung

Travere Therapeutics in San Diego, with remote options in the USA, is seeking an Associate Director, Clinical Science to advance clinical development programs and lifecycle activities. You will work with cross-functional teams to design trials, analyze data, and prepare regulatory submissions.

Ideal candidates hold a PhD/PharmD/MD, have 4+ years in pharma, and experience with clinical trials and regulatory documents. Domestic and international travel up to 15% is required.

Qualifikationen

• PhD/PharmD/MD in a related life science discipline required; equivalent combination may be considered.
• 4+ years of relevant experience in the pharmaceutical industry; experience in rare disease preferred.
• Experience supporting clinical trials and clinical studies.

Aufgaben

• Lead clinical science components of study plans and protocol design.
• Review and summarize clinical trial safety and efficacy data for team discussions.
• Coordinate timelines and deliverables across study teams with accurate documentation.
• Support study conduct in accordance with protocols and GCP.
• Lead preparation and scientific review of reports, slides, and ClinicalTrials.gov summaries.
• Contribute to INDs, NDAs, BLAs, regulatory submissions and related documents.
• Build relationships with alliance partners, investigators, and key opinion leaders.
• Contribute to manuscripts and scientific presentations.

Ausbildung

PhD/PharmD/MD in life sciences

Clinical trials experience

Jobbeschreibung

Travere Therapeutics in San Diego, with remote options in the USA, is seeking an Associate Director, Clinical Science to advance clinical development programs and lifecycle activities. You will work with cross-functional teams to design trials, analyze data, and prepare regulatory submissions.

Ideal candidates hold a PhD/PharmD/MD, have 4+ years in pharma, and experience with clinical trials and regulatory documents. Domestic and international travel up to 15% is required.