Remote Senior Clinical Science Lead, Orexin Trials

100 Eli Lilly and Company

United States

Remote

USD 168.000 - 284.000

Vollzeit

Vor 10 Tagen

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Benefits dieser Stelle

401(k) plan
Health benefits
Vacation benefits
Flexible benefits

Zusammenfassung

Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, seeks a Senior Advisor, Clinical Science to provide scientific leadership for early-stage (Phase 1/2) trials in orexin-targeted programs related to neurodegeneration and neuropsychiatric indications.

You will lead cross-functional teams, design studies, review safety/PK/ biomarker data, and mentor junior scientists while collaborating with Regulatory, Biostatistics, and Translational Science to deliver high-quality

Qualifikationen

  • Advanced degree in science/clinical field with PhD or PharmD preferred.
  • 8–10 years in clinical research or development in biotech/pharma.
  • Strong neuroscience/neurology foundation; experience in neurodegeneration/neuropsychiatric indications desired.
  • Experience leading development and authorship of clinical and regulatory documents.

Aufgaben

  • Serve as clinical scientist lead on one or more early-stage trials (Phase 1/2) for Orexin-targeted programs.
  • Contribute to clinical development plan strategy, study design, dose-escalation strategies, and data interpretation.
  • Lead development and review of key documents (protocols, IBs, CSRs, regulatory briefs).
  • Lead study medical/scientific activities from start-up to CSR completion and data interpretation.
  • Collaborate with cross-functional teams to ensure high-quality, timely trial delivery.

Kenntnisse

Clinical trial design
Neurodegeneration expertise
Data interpretation
Cross-functional leadership
Scientific writing
Orexin biology knowledge

Ausbildung

PhD or PharmD

Jobbeschreibung

Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, seeks a Senior Advisor, Clinical Science to provide scientific leadership for early-stage (Phase 1/2) trials in orexin-targeted programs related to neurodegeneration and neuropsychiatric indications.

You will lead cross-functional teams, design studies, review safety/PK/ biomarker data, and mentor junior scientists while collaborating with Regulatory, Biostatistics, and Translational Science to deliver high-quality

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