Senior Scientific Director, Oncology Clinical Development (Non-Hodgkin Lymphoma)
Core
Leads the design, implementation, and interpretation of clinical development programs for oncology molecules, specifically Non-Hodgkin Lymphoma, ensuring data supports product strategy.
Role type
Senior Scientific Director, Oncology Clinical Development
Builds
Clinical development plans, protocols, Investigator Brochures, Clinical Study reports, and regulatory submissions for oncology assets.
Domain
Pharmaceutical industry, Oncology, Hematology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial methodology, regulatory compliance, study protocol design, safety and efficacy data interpretation, cross-functional team leadership, Good Clinical Practices (GCP), pharmacovigilance standards, strategic planning, external opinion leader engagement.
Preferred skills
Advanced degree (MS, PhD), Hematology experience, Non-Hodgkin Lymphoma (NHL) experience.
Technologies
Clinical trial management systems, regulatory submission platforms.
Responsibilities
Lead and own the design and implementation of multiple clinical development programs; oversee project-related education of investigators and study staff; ensure study enrollment and timelines; serve as clinical expert for molecules and diseases; participate in due diligence or business development activities; represent the company at external meetings; ensure adherence to quality standards and regulatory requirements.
Seniority
Senior, hands-on IC with leadership responsibilities