Therapeutic Area Medical Lead - Oncology - Sponsor dedicated (m/w/d)

Overview

The Therapeutic Area Lead Solid Tumors / Pipeline is part of the Medical Affairs Team and provides a bridge between Clinical Development, Medical Affairs, and the commercial organization at a senior mastery level.

The role involves a variety of activities for inline and pipeline products across multiple therapeutic areas, providing medical insights and in-depth market understanding based on related IT analysis of the assigned indications.

Responsibilities

• Build and maintain expertise in the assigned tumor entities and products, reviewing literature, treatment options, disease environment, and product data.
• Act as primary training and educational contact, delivering content and providing expertise to internal and external stakeholders.
• Analyze data from early development indications, produce meaningful reports and derive strategies.
• Identify and engage internal and external experts for medical communications and content development.
• Oversee preparation and delivery of high‑quality content and educational materials, including medical society presence, abstracts, and publications.
• Develop and execute multi‑channel communication strategies and educational event planning.
• Serve as medical point of contact for clinical studies within solid tumor indications and support study centers and the Clin Ops team.
• Screen the German medical landscape for key opinion leaders and research groups in relevant indications.
• Participate in cross‑functional medical planning, working groups, and task forces.
• Account for congress medical communication activities and participate in reporting and summaries.
• Serve as Information Officer, ensuring proper pre‑medical review of materials.
• Drive implementation of medical/non‑promotional plans for products and provide input into local brand planning.
• Ensure educational activities are scientifically high quality, compliant with regulations and company guidelines.
• Contribute to strategic medical plans, updating them as needed.
• Manage resources within the annual medical affairs brand budget.
• Provide medical leadership for market‑access dossiers.
• Oversee agenda development, content creation, and execution for educational symposia, internal meetings, advisory boards, investigator meetings, and clinical presentations at medical meetings.
• Support content development and deliver presentations, briefing documents, FAQs, backgrounders, newsletters, slide decks, and medical information letters.

Qualifications

• MD, Pharm D, or Ph D in life sciences.
• 5–7 years of experience in oncology within the pharmaceutical industry.
• Proven track record in product launch preparation and life‑cycle management.
• Experience in developing and implementing clinical trials.
• Experience as an Information Officer reviewing medical materials.
• Excellent communication skills and ability to present scientific data.
• Structured project management approach, able to work independently in complex, rapidly changing environments.
• Analytical mindset, entrepreneurial approach, hands‑on attitude.
• Willingness to travel up to 25% of working time.
• Good spoken and written German and English.
• Proficiency with Veeva, Microsoft Office, and relevant public medical data sources.
• Hybrid role – attend office 2–3 times per week.
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