- External
- Germany
Job Title: Medical Director – Immuno-Oncology
(Vice President title available for highly experienced candidates)
Location: Germany (Hybrid/Remote options available)
Reports To: Chief Medical Officer (CMO)
About the Company
Join a cutting-edge biotechnology company focused on developing transformative oncology therapies that improve patient outcomes. With a strong culture of innovation and scientific excellence, our client is shaping the next generation of cancer treatments.
We are passionate about making a meaningful impact—and we’re looking for a visionary Medical Director to help us lead the future of immuno-oncology.
The Role: Medical Director – Immuno-Oncology
In this high-impact leadership role, you will oversee the clinical development strategy for our oncology portfolio. You’ll collaborate with cross-functional teams, lead clinical trials, and engage with global regulatory bodies. From early-stage development to pivotal trials, your work will directly support breakthrough cancer therapies.
Key Responsibilities
Clinical Development Strategy
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Lead strategic planning for oncology clinical trials.
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Align development activities with corporate goals and patient needs.
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Design clinical studies and prepare regulatory submission plans.
Clinical Trial Oversight
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Provide expert medical leadership for Phase 1–3 trials.
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Monitor trial progress and interpret data to inform decision-making.
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Ensure compliance with international regulatory standards.
Cross-Functional Collaboration
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Partner with Clinical Operations, Regulatory, Safety, and Commercial teams.
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Translate data into practical, patient-focused treatment strategies.
Regulatory and Compliance
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Oversee preparation of CTAs, INDs, and global submission materials.
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Ensure adherence to EMA, FDA, ICH-GCP, and other regulatory standards.
KOL and Investigator Engagement
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Cultivate relationships with key opinion leaders and principal investigators.
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Represent the company at advisory boards, investigator meetings, and conferences.
Medical Affairs Leadership
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Act as a medical spokesperson both internally and externally.
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Integrate emerging science and clinical insights into strategy.
Data Analysis and Interpretation
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Review and interpret trial data for internal and external audiences.
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Provide clear, actionable recommendations based on clinical evidence.
Team Leadership
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Mentor and lead a team of clinical professionals.
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Foster a collaborative and scientifically rigorous team culture.
What We’re Looking For
Education
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MD (or equivalent); PhD or MBA is a plus.
Experience
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8–10 years in clinical research, with 5+ years in oncology clinical development.
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Proven leadership in designing and managing oncology trials.
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Experience with regulatory submissions and agency interactions (FDA, EMA, etc.).
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Deep knowledge of molecular oncology, immuno-oncology, biomarkers, and targeted therapies.
Skills
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Strong communication and stakeholder engagement.
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Ability to translate complex science into strategic plans.
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Fluent in English; additional European languages are a plus.
Personal Attributes
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Strategic thinker with strong analytical skills.
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Detail-oriented and regulatory-savvy.
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Collaborative leader who thrives in dynamic environments.
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Patient-focused and committed to improving cancer care.
Benefits and Compensation
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Competitive salary and bonus structure
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Comprehensive benefits package (healthcare, retirement plans, etc.)
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Opportunities for career advancement in a rapidly growing company
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Flexible working arrangements and a supportive, inclusive work culture
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The chance to work on pioneering oncology therapies that can transform patient outcomes
If you’re ready to lead transformative change in cancer treatment, apply now and be part of a company that’s redefining what’s possible in oncology.