Work Your Magic with us! Start your next chapter and join EMD Serono.

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

As a Medical Director in Global Clinical Development Oncology, you will provide clinical and scientific leadership for development programs in oncology, ideally with experience in targeted therapies, antibody-drug conjugates (ADCs), and/or immuno-oncology. Next to experience with drug development for solid tumors, experience with hematology/hematologic oncology is viewed favorably.

In this role, you will independently drive day-to-day clinical development activities while contributing to high-quality execution of the overall clinical strategy in a global matrix environment.

Key Accountabilities:

* Lead assigned clinical studies and contribute to broader program strategy across the development continuum, from Phase 1 through Phase III, including support for registration-enabling activities, regulatory submissions, and Health Authority interactions.
* Integrate clinical, translational, biomarker, and emerging data to support indication strategy, patient selection, dose strategy, and key development decisions.
* Operate as a core member of cross-functional teams and the Global Project Team, partnering closely with Program Leadership and Management, Translational Medicine, Biostatistics, Clinical Pharmacology, Regulatory Affairs, Clinical Operations, Safety, and Medical Writing.
* Support study design, dose strategy, patient selection, and indication prioritization
* Integrate clinical, translational, and biomarker data into development decisions
* Provide medical monitoring and clinical oversight for assigned studies
* Review and interpret safety and efficacy data to support study decisions
* Author and contribute to key clinical and regulatory documents, including protocols, investigator brochures, clinical study reports, briefing books, submission documents, and dossiers
* Contribute to registration-enabling activities and regulatory submissions
* Support interactions with Health Authorities and internal governance bodies
* Drive execution of deliverables across global teams and timelines
* Contribute to a high-performing, collaborative matrix environment.

Who You Are

Minimum Qualifications:

* MD with expertise in clinical
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