Senior Medical Director, Oncology & Prostate Cancer

Delphia Therapeutics, Inc.; Cambridge (MA); Vor Ort; USD 290.000 - 320.000; Vollzeit

Zusammenfassung

Delphia Therapeutics, Inc. in Cambridge, MA is seeking a Senior Medical Director to lead clinical development in oncology, translating preclinical insights into development strategies from discovery through proof-of-concept and registration.

Reporting to the Chief Medical Officer, you will serve as Medical Monitor, ensure patient safety across assets, and collaborate with Clinical Operations, Regulatory Affairs, Biostatistics, and Translational Medicine, with a focus on prostate cancer

Qualifikationen

• MD with significant oncology clinical development experience and medical monitoring.
• 3+ years of industry experience, preferably in biotech.
• Hands-on oncology trial design, execution, and monitoring.
• Strong clinical judgment interpreting complex oncology data.
• Knowledge of FDA and ICH oncology regulations.
• Ability to work independently in a fast-paced, matrixed environment.
• Excellent collaboration and communication across stakeholders.

Aufgaben

• Lead design, execution, and oversight of oncology trials Phase 1–3.
• Serve as Medical Monitor ensuring study integrity and safety signals.
• Interpret data and translate into actionable development insights.
• Ensure timely completion of trial documents and regulatory submissions.
• Collaborate with safety team to analyze SAEs and safety signals.
• Stay current on care standards and competitive landscape.
• Build relationships with investigative sites and KOLs.
• Collaborate cross-functionally to advance programs.

Kenntnisse

Medical monitoring

Cross-functional leadership

Oncology clinical development

Trial design and execution

Data interpretation

Regulatory knowledge

Stakeholder engagement

Ausbildung

MD ( oncology focused)

Jobbeschreibung

Delphia Therapeutics, Inc. in Cambridge, MA is seeking a Senior Medical Director to lead clinical development in oncology, translating preclinical insights into development strategies from discovery through proof-of-concept and registration.

Reporting to the Chief Medical Officer, you will serve as Medical Monitor, ensure patient safety across assets, and collaborate with Clinical Operations, Regulatory Affairs, Biostatistics, and Translational Medicine, with a focus on prostate cancer