Director, Clinical Scientist – Solid Tumors

0750 Stemline Therapeutics Inc

New York (NY)

Presencial

USD 173.000 - 255.000

Jornada completa

Hace 8 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

0750 Stemline Therapeutics Inc in New York is seeking a Clinical Scientist (Director/Senior Director) to lead and contribute to the development and execution of solid tumor oncology programs. You will work in a matrix environment with cross‑functional teams, supporting study design, data interpretation, and regulatory submissions.

The role requires 5+ years in drug development as a clinical scientist, advanced degree, and proficiency with EDC systems and regulatory guidelines.

Formación

  • 5+ years’ experience in drug development as a clinical scientist or related role in pharmaceutical/biotech industry.
  • Knowledge of GCP, ICH Guidelines and current US FDA regulations.
  • Willingness to work Eastern Time Zone (US) hours.

Responsabilidades

  • Plan, execute, and report clinical trials, primarily in oncology.
  • Contribute to study protocols, ICFs/amendments and regulatory documents.
  • Collaborate with external partners and study committees.
  • Develop and present training materials and study data at meetings and conferences.
  • Support trial operations, including CRF design and TMF submissions.

Conocimientos

Clinical Data Review
Regulatory Knowledge
Cross-functional Collaboration
EDC Systems

Educación

Advanced degree (MS, PharmD, PhD)

Herramientas

Medidata RAVE

Descripción del empleo

0750 Stemline Therapeutics Inc in New York is seeking a Clinical Scientist (Director/Senior Director) to lead and contribute to the development and execution of solid tumor oncology programs. You will work in a matrix environment with cross‑functional teams, supporting study design, data interpretation, and regulatory submissions.

The role requires 5+ years in drug development as a clinical scientist, advanced degree, and proficiency with EDC systems and regulatory guidelines.

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