Director, Clinical Scientist – Solid Tumors

MENARINI Group

United States

Remote

USD 173.000 - 255.000

Vollzeit

Vor 8 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

401(k) with company match
Health insurance
Life & AD&D insurance
FSA/HSA programs

Zusammenfassung

Stemline Therapeutics Inc. seeks a Clinical Scientist (Director/Senior Director) to lead the planning, execution, and reporting of oncology clinical trials within a matrix, cross-functional setting.

The role partners with Medical Directors to design studies and deliver on programs, contributing to regulatory submissions and data interpretation. Based in the United States, the position involves collaboration with external partners, study committees, and dissemination of findings at scientific

Qualifikationen

  • 5+ years’ experience in drug development as a clinical scientist or related role.
  • Advanced degree (MS, PharmD, PhD) or equivalent.
  • Experience in late phase solid tumor oncology.
  • Proficient with Microsoft Word/Excel/PowerPoint, EDC systems (Medidata RAVE), and data review tools.
  • Knowledge of GCP, ICH Guidelines and current US FDA regulations.
  • Willingness to work Eastern Time Zone (US) hours.

Aufgaben

  • Plan, execute, and report clinical trials, primarily in oncology.
  • Collaborate with cross-functional teams to ensure data integrity and safety.
  • Contribute to study design, protocols, and regulatory submissions.
  • Develop and deliver training materials and presentations.
  • Support trial operations and ensure alignment with protocol and TMF requirements.

Ausbildung

Advanced degree (MS, PharmD, PhD) or equivalent

Tools

EDC systems (Medidata RAVE)
MS Word/Excel/PowerPoint
Data review tools

Jobbeschreibung

Stemline Therapeutics Inc. seeks a Clinical Scientist (Director/Senior Director) to lead the planning, execution, and reporting of oncology clinical trials within a matrix, cross-functional setting.

The role partners with Medical Directors to design studies and deliver on programs, contributing to regulatory submissions and data interpretation. Based in the United States, the position involves collaboration with external partners, study committees, and dissemination of findings at scientific

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