Remote Senior Medical Director, Oncology & Hematology

TFS HealthScience; Lisboa; Presencial; EUR 150 000 - 210 000; Tempo integral

Resumo da oferta

TFS HealthScience invites applications for a Senior Medical Director, based at home in Europe (Spain, Germany, Sweden, UK, Poland or Portugal). The role blends medical monitoring with portfolio-level medical oversight to uphold scientific credibility for current and future sponsors in oncology/hematology.

Key responsibilities include leading medical monitor activities, providing senior medical input on study design, safety reviews, and regulatory documentation, and mentoring junior staff while

Qualificações

• MD degree and specialist medical training.
• 10+ years of post‑qualification medical experience.
• 7+ years in oncology/haematology clinical development and senior Medical Director experience in CRO/biotech/pharma.

Responsabilidades

• Serve as medical monitor for oncology studies, including protocol-related medical reviews and safety data assessment.
• Provide medical oversight across the oncology portfolio and act as escalation point for studies in delivery.
• Offer medical input on study design and measurements in trials and review safety sections of protocols and Investigator’s Brochure.
• Review safety data listings (adverse events, labs, vital signs, ECGs) and safety reports (DSURs, PSURs, PBRERs).
• Contribute to regulatory documents and literature review; participate in SOPs and tools development.
• Provide education and supervision to junior Medical Advisors and Medical Directors.

Conhecimentos

Medical leadership

Oncology expertise

Clinical monitoring

Formação académica

MD degree

Specialist medical training

Descrição da oferta de emprego

TFS HealthScience invites applications for a Senior Medical Director, based at home in Europe (Spain, Germany, Sweden, UK, Poland or Portugal). The role blends medical monitoring with portfolio-level medical oversight to uphold scientific credibility for current and future sponsors in oncology/hematology.

Key responsibilities include leading medical monitor activities, providing senior medical input on study design, safety reviews, and regulatory documentation, and mentoring junior staff while