Oncology Clinical Program Lead (Hybrid)

Novartis Group Companies

East Hanover (NJ)

Hybrid

USD 249.000 - 462.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Novartis Group of Companies in Cambridge, MA seeks a Senior CPL to provide strategic medical guidance and lead the development of experimental oncology agents from PE/DC through TDP, collaborating across functions and geographies.

The role requires an MD or DO with board certification in oncology (PhD preferred), fluent English, and a track record in oncology trials, preclinical data interpretation, PK/PD concepts, and writing and presenting scientific data to diverse audiences.

Qualifikationen

  • MD or DO degree required.
  • Board-certification in oncology; PhD preferred.
  • Fluent English - oral and written.
  • 2+ years pharma/biotech oncology trials or equivalent academic translational oncology.
  • Experience with PK/PD and biostatistics in clinical development.
  • Strong written and oral communication skills.

Aufgaben

  • Provide strategic medical leadership across the project team for preclinical to clinical oncology development.
  • Create clinical development strategies from PE/DC to TDP in collaboration with multidisciplinary teams.
  • Develop Integrated Development Plans aligning with DALs, DEV, S&G, and Commercial teams.
  • Lead Biomedical Research Early Program Teams to support clinical development and trials.
  • Integrate preclinical data to inform clinical development decisions and protocols.
  • Collaborate with clinical scientists to develop protocols and reports for trials.
  • Ensure adherence to GCP and Novartis SOPs; maintain regulatory compliance.

Ausbildung

MD or DO degree
Board-certification in oncology
PhD-level science preferred
Fluent English - Oral and written
Leadership in translational oncology
Excellent medical/scientific writing

Jobbeschreibung

Novartis Group of Companies in Cambridge, MA seeks a Senior CPL to provide strategic medical guidance and lead the development of experimental oncology agents from PE/DC through TDP, collaborating across functions and geographies.

The role requires an MD or DO with board certification in oncology (PhD preferred), fluent English, and a track record in oncology trials, preclinical data interpretation, PK/PD concepts, and writing and presenting scientific data to diverse audiences.

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