Medical Advisor Oncology

Job Description Summary

Job Description

Major Accountabilities

Medical Strategy & Scientific Leadership

• Contribute to the design execution and monitoring of the local Medical Affairs plan in alignment with global and regional medical strategies.
• Act as a scientific reference for the assigned Therapy Area ensuring medical activities are patientcentric evidencebased and nonpromotional.

Scientific Exchange & Stakeholder Engagement

• Establish and maintain highquality scientific dialogue with Key Opinion Leaders (KOLs) investigators scientific societies and relevant regulatory or public health stakeholders.
• Support scientific meetings advisory boards and educational initiatives in compliance with internal governance and external regulations.
• Medical Information & Scientific Accuracy : Ensure timely accurate and highquality responses to medical inquiries in accordance with applicable standards and SOPs.

Clinical Research & Evidence Generation

• Provide medical and scientific input into the planning initiation execution and oversight of clinical research activities including:
  • NonInterventional Studies (NIS)
  • InvestigatorInitiated Trials (IITs)
  • RealWorld Evidence (RWE) initiatives
• Support country evidence generation strategy in alignment with global guidance and local priorities.

CrossFunctional Collaboration & Insights

• Provide medical insights to crossfunctional stakeholders including Pharmacovigilance Regulatory Affairs Market Access Quality Commercial and Brand teams.
• Ensure systematic collection documentation and communication of medical insights to inform strategy and decisionmaking.

Medical Governance & Compliance

• Coordinate medical review and approval of locally developed and global medical materials in accordance with Medical Governance and local SOPs.
• Ensure clear separation between promotional and nonpromotional activities.
• Identify assess and mitigate medical and compliance risks within the scope of responsibility ensuring appropriate internal controls are implemented and monitored.

Patient Safety & Quality

• Ensure reporting of adverse events technical complaints and special case scenarios within 24 hours in line with Pharmacovigilance requirements.
• Support quality and safety culture across all medical activities.

Key Performance Indicators (KPIs)

• Compliance with Ethics Compliance Medical Governance and SOP requirements.
• Quality and scientific rigor of medical activities and deliverables.
• Effective contribution to medical strategy execution and evidence generation.
• Timely and accurate medical information responses.
• Quality of crossfunctional collaboration and medical insights shared.

Minimum Requirements

Education & Experience

• Medical pharmacy (preferred) or lifescience degree (MD PharmD PhD or equivalent).
• Experience in Medical Affairs Clinical Research or related scientific roles within the pharmaceutical or healthcare environment.
• Demonstrated experience in crossfunctional collaboration and project execution.

Core Competencies & Skills

• Medical & scientific expertise in the assigned Therapy Area.
• Clinical research and evidence generation knowledge.
• Strong understanding of Medical Affairs governance compliance and pharmacovigilance.
• Strategic thinking and analytical skills.
• Excellent communication and stakeholder engagement capabilities.
• Project management and organizational skills.

Languages

• English French (fluent)

Skills Desired