Senior Medical Director, Oncology Clinical Development

Scorpion Therapeutics; Cambridge (MA); On-site; USD 320,000 - 520,000; Full time

Job summary

Scorpion Therapeutics in Cambridge, MA seeks a Senior Medical Director to lead late-stage oncology development, focusing on pivotal Phase III trials and registration studies.

You will provide medical leadership for trial design, act as Medical Monitor, engage with investigators and regulators, analyze efficacy and safety data, and drive lifecycle strategies with cross-functional teams.

Qualifications

• MD with board certification in Oncology or Hematology-Oncology, 5+ years in late-stage oncology development.
• Experience in trial design and Medical Monitor oversight.
• Regulatory submissions experience.

Responsibilities

• Provide medical leadership for trial design and oversight as Medical Monitor, support regulatory submissions and cross-functional collaboration.
• Serve as external representative and build relationships with investigators, KOLs, and regulators.
• Analyze clinical data for efficacy and safety insights, develop lifecycle strategies, and support regulatory interactions.

Skills

Medical leadership

Cross-functional collaboration

Regulatory interactions

Data analysis

Medical monitoring

Education

MD with board certification in Oncology

Job description

Role: Lead late-stage clinical development in Oncology as Senior Medical Director, focusing on pivotal Phase III trials and registration studies.

Responsibilities

• provide medical leadership for trial design, oversight as Medical Monitor, contribute to regulatory submissions, support commercialization, and collaborate cross-functionally with clinical operations, regulatory affairs, pharmacovigilance, biostatistics, and medical affairs
• Serve as external representative and build relationships with investigators, KOLs, and regulators
• Analyze clinical data for efficacy and safety insights, develop lifecycle strategies, and support regulatory interactions

Qualifications

• MD with board certification in Oncology or Hematology-Oncology; 5+ years in clinical development, particularly late-stage oncology trials

Preferred

• proven track record as Medical Monitor, regulatory submission success, deep understanding of oncology drug development, clinical endpoints, and pathways, with strong leadership and collaboration skills

High-Value

• oncology, late-stage development, Phase III, clinical trial leadership, medical monitoring, regulatory support, international collaboration, travel up to 30%, based in Cambridge, MA