Medical Director (Europe)

Das ist der Job

We also operate GMP manufacturing to produce individualized N=1 therapeutics.

Darum lohnt es sich

You will work at the interface of treating physicians, molecular tumor boards, bioinformatics, AI/ML, wet‑lab teams and external diagnostic partners.

Depending on the candidate profile, the role may start as a part‑time, fractional or advisory engagement and evolve into a broader permanent leadership role. /b /p h3WHAT YOU’LL DO /h3 ul liProvide medical and oncological oversight for DAiNA’s patient‑specific precision‑oncology cases. /li liReview medical records, pathology reports, treatment histories, imaging summaries and other clinical information for completeness, relevance and clinical context. /li liReview and contribute to clinical case summaries, molecular interpretation reports and therapy‑relevant recommendations. /li liProvide medical review and sign‑off for DAiNA reports where appropriate, ensuring clarity, medical accuracy and clinical relevance. /li liTranslate multi‑omics findings, liquid‑biopsy signals and ex‑vivo functional testing results into oncologically meaningful hypotheses and options for discussion with treating physicians. /li liInterface with treating physicians, external oncologists and molecular tumor boards, including preparation and follow‑up of case discussions. /li liSupport clinical risk assessment, patient‑safety considerations and appropriate boundaries between scientific interpretation, decision support and medical treatment responsibility. /li liContribute to DAiNA’s broader clinical strategy, including personalized therapeutics, monitoring concepts, real‑world evidence generation and future clinical validation. /li /ul h3WHAT YOU BRING /h3 ul liLicensed physician, M.D. or equivalent, with board certification or advanced specialization in medical oncology, hematology/oncology or a closely related cancer‑focused discipline. /li liExperience using molecular diagnostics, genomic profiling or molecular tumor boards to inform cancer treatment decisions. /li liStrong understanding of modern precision oncology, including genomic alterations, pathway biology, targeted therapies, immuno‑oncology and resistance mechanisms. /li liExperience reviewing clinical documentation and translating complex medical information into clear, structured and clinically useful summaries. /li liInterest in building clinical governance, reporting standards and medically robust workflows in an early‑stage precision‑oncology company. /li /ul h3NICE TO HAVE /h3 ul liExperience with molecular tumor boards, precision‑oncology programs, comprehensive genomic profiling or advanced diagnostic workups. /li liExperience with personalized therapeutics, neoantigen vaccines, cell therapies, RNA‑based therapeutics, individualized treatment concepts or N=1 approaches. /li liPrevious experience in clinical study design, real‑world evidence generation, patient registries or clinical validation of diagnostic/decision‑support platforms. /li /ul h3WHY DAINA /h3 ul liEmployer contributions toward private health insurance or supplementary health coverage, as well as pension or retirement savings. /li liPerformance‑based bonus opportunity, depending on company and individual performance. /li liHybrid model with ~60% of working time expected on‑site and the rest remotely, depending on team and business needs. /li liA personal development budget for conferences, courses, certifications, and training. /li liThe opportunity to work directly on real patient cases and help shape a first‑in‑class precision‑oncology platform. /li liA proactive, collaborative team with fast decision‑making and strong ownership of your domain. /li /ul h3HOW TO APPLY /h3 pbSend your CV and a short note on why this role fits you to , quoting “Medical Director” in the subject line. ppbLocation: Berlin, Germany or Zurich area /b /p pbType: Permanent (full- or part-time)/ advisory possible to start /b /p pbStart Date: As soon as possible / by arrangement /b /p h3ABOUT DAiNA /h3 pbDAiNA is a precision‑oncology company focused on enabling personalized cancer treatment for individual patients.

We combine comprehensive molecular tumor data including genomics, transcriptomics (bulk, single cell and spatial), proteomics and epigenetics, with AI‑driven analysis.

Our platform connects multi‑omic profiling with functional ex‑vivo tumor models and personalized liquid‑biopsy monitoring, creating a continuous workflow from biopsy and treatment selection through to therapy monitoring and adaptation.

In short, we help physicians make more informed, personalized treatment decisions based on high‑dimensional molecular tumor data. For more information, visit: /b /p h3THE ROLE /h3 pbAs Medical Director, you will provide the clinical and oncological leadership for DAiNA’s precision‑oncology cases.

You will ensure that each patient case is reviewed, interpreted and communicated in a medically sound, clinically relevant and quality‑controlled manner.

Your role is to bring clinical context into DAiNA’s multi‑omics and functional testing workflow, helping translate complex molecular and ex‑vivo data into meaningful options for personalized cancer treatment. This position is central to building DAiNA’s clinical governance, medical review and reporting standards.

We review applications on a rolling basis and aim to reply quickly. /b /p pbDAiNA is an equal‑opportunity employer. We welcome applicants of every background and assess every candidate on merit, regardless of age, gender, ethnicity, religion, disability, sexual orientation or origin.

If you need any adjustment to the process, let us know in your application. /b /p /p