Chief Oncology Medical Director

Avance Clinical Pty Ltd.; United States; Sur place; USD 230 000 - 360 000; Plein temps

Avantages offerts par ce poste

Salary package

Flexible work

Tech systems

Challenging projects

Career progression

Supportive leadership

Global CRO stability

Résumé du poste

Avance Clinical is seeking a Medical Director in Oncology to provide medical and scientific leadership across oncology clinical development programs. The role involves serving as Medical Monitor, guiding protocol design, safety oversight, and cross-functional collaboration to ensure data quality and patient safety in all phases of oncology research.

You will engage with sponsors, investigators, and internal teams, contributing to business development through proposals and meetings, and mentoring

Qualifications

• Medical degree (MD or equivalent) required.
• Specialist training, board certification, fellowship, or equivalent qualification in Oncology preferred.
• Significant experience in oncology clinical research in CRO/pharma/academic settings.
• Experience as Medical Monitor or medical oversight for oncology trials.

Responsabilités

• Provide medical and scientific leadership for oncology programs as Medical Monitor and SME.
• Review eligibility, protocol compliance, safety events, and data integrity.
• Input on dose-escalation decisions and safety/oversight committees.
• Support investigators with protocol inquiries and clinical guidance.
• Deliver oncology expertise across study teams and departments.
• Contribute to protocol/informed consent and study documents.
• Advise on patient populations, endpoints, and safety monitoring.

Connaissances

Medical leadership

Oncology expertise

Data interpretation

Regulatory knowledge

Team mentoring

Sponsor interactions

Cross-functional collaboration

Communication skills

Formation

MD or equivalent

Board/Fellowship in Oncology

Description du poste

Avance Clinical is seeking a Medical Director in Oncology to provide medical and scientific leadership across oncology clinical development programs. The role involves serving as Medical Monitor, guiding protocol design, safety oversight, and cross-functional collaboration to ensure data quality and patient safety in all phases of oncology research.

You will engage with sponsors, investigators, and internal teams, contributing to business development through proposals and meetings, and mentoring