Global Oncology Medical Director — Clinical Development

Barrington James; Boston (MA); On-site; USD 250,000 - 350,000; Full time

Job summary

The position offers office-based work, with responsibilities spanning protocol authoring, biomarker integration, and regulatory submissions. English communication and board-certified oncology expertise are essential.

Qualifications

• MD with oncology-focused clinical drug development expertise.
• Experience supporting or leading trial programs from Phase 1 to Phase III.
• Familiarity with regulatory submissions and health authority interactions.
• Ability to integrate translational/biomarker data into development decisions.

Responsibilities

• Lead assigned clinical studies and contribute to program strategy from Phase 1 to Phase III.
• Integrate clinical, translational, biomarker data to support indication and dose strategy.
• Collaborate with cross-functional teams and Global Project Team across functions.
• Provide medical monitoring and oversight for studies and safety reviews.
• Draft and contribute to protocols, ICH documents, and regulatory submissions.
• Support interactions with Health Authorities and governance bodies.
• Drive milestones across global teams and timelines.
• Maintain high standards of scientific integrity and leadership.

Skills

Clinical drug development

Oncology expertise

Cross-functional collaboration

English communication

Medical writing

Education

MD

Job description

The position offers office-based work, with responsibilities spanning protocol authoring, biomarker integration, and regulatory submissions. English communication and board-certified oncology expertise are essential.