20 beste Stellen als p2607 medical director, oncology in lausanne vd – aktuell auf Personalsuche

P2607 - Medical Director, Oncology
Debiopharm —Lausanne, VD
- 100%
- Master
Direkt bewerben
Medical Director, Oncology
Debiopharm —Lausanne, VD
- 100%
Senior Medical Director, Global Risk Management & Safety Surveillance
Incyte Corporation —Morges, VD
- Doktorat
Director Group Patents
Ferring Pharmaceuticals, Inc. —Saint-Prex, VD
- 100%
P2614 - Pharmaceutical Quality (pQM) Specialist
Debiopharm —Lausanne, VD
- 100%
- Englisch
- Analysefähigkeit
- Bachelor
Direkt bewerben
Global Early Commercial Manager, Oncology
Debiopharm —Lausanne, VD
- 100%
- Doktorat
- Master
- Bachelor
P2606 - Global Early Commercial Manager, Oncology
Debiopharm —Lausanne, VD
- 100%
- Doktorat
- Master
- Bachelor
Direkt bewerben
P2613 - CSV Lead
Debiopharm —Lausanne, VD
- 100%
- Englisch
- Master
- Analysefähigkeit
Direkt bewerben
Product Manager - Spatial Biology
Bio-Techne —Tolochenaz, VD
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Management-Erfahrung
3 Tage
EHS Expert - All Genders
Merck KGaA —Corsier-sur-Vevey, VD
- Aufstiegsmöglichkeiten
3 Tage
Principal Clinical Pharmacologist
Debiopharm —Lausanne, VD
- 100%
- Doktorat
- Englisch
- Kommunikationsfähigkeit
P2611 - Senior Legal Counsel - Commercial & Privacy
Debiopharm —Lausanne, VD
- 100%
- Englisch
- Master
Direkt bewerben
P2609 - Senior Trial Master File (TMF) Specialist
Debiopharm —Lausanne, VD
- 100%
- Microsoft Excel
- Englisch
- Master
Direkt bewerben
P2604 - Principal Clinical Pharmacologist
Debiopharm —Lausanne, VD
- 100%
- Doktorat
- Englisch
- Kommunikationsfähigkeit
Direkt bewerben
Internship - Automatic Document Extraction (m/f/d)
Merck KGaA —Corsier-sur-Vevey, VD
- Englisch
- Analysefähigkeit
- Praktikum
- Aufstiegsmöglichkeiten
P2618 - Global Value & Access Lead
Debiopharm —Lausanne, VD
- 100%
- Hybrides Arbeiten
- Management-Erfahrung
- Master
- Analysefähigkeit
Direkt bewerben
9 Tage
Internship: Autonomous Downstream Purification for Monoclonal Antibodies (m/fd)
Merck KGaA —Corsier-sur-Vevey, VD
- Englisch
- Praktikum
- Python
- Aufstiegsmöglichkeiten
Internship - Microbiology Quality Control (m/f/d)
Merck KGaA —Corsier-sur-Vevey, VD
- Englisch
- Praktikum
- Aufstiegsmöglichkeiten
6 Tage
Project Scheduler/Steerer (CDM 18 months) - All Genders
Merck KGaA —Aubonne, VD
- Zweisprachig
- Englisch
- Master
- Aufstiegsmöglichkeiten
P2612 - Senior Manager Statistical Programming
Debiopharm —Lausanne, VD
- 100%
- Informatik
- Master
- Softwareentwicklung
Direkt bewerben

Ich möchte aktuelle Job-E-Mails für Stellen als p2607 medical director, oncology in lausanne vd erhalten

Wenn Sie sich bei Ihrem Konto anmelden, stimmen Sie den Nutzungsbedingungen, den Richtlinien zur Verwendung von Cookies sowie der Datenschutzerklärung von SimplyHired zu.

Weitere Job-Standorte erkunden

p2607 medical director, oncology jobs near lausanne vd

Jobs als Director Of Risk Management in Zürich, Zh

Jobs als Director Of Risk Management in Genf, Ge

Jobs als Senior Risk Manager in Zürich, Zh

Jobs als Commercial Manager in Zürich, Zh

Jobs als Commercial Manager in Luzern, Lu

Jobs als Account Manager in Zürich, Zh

Jobs als Commercial Manager in Allschwil, Bl

Jobs als Hotel Manager in Zürich, Zh

Jobs als Quality Specialist in Basel, Bs

Jobs als Master Data Specialist in Kanton Zürich

Jobs als Customer Experience Specialist in Bern, Be

Jobs als Quality Specialist in Bulle, Fr

Jobs als Quality Specialist in Baden, Ag

Jobs als Sales Manager in Basel, Bs

Jobs als Category Manager in Zürich, Zh

Jobs als Quality Control Associate in Stein Ag, Ag

Jobs als Manager Automotive in Kanton Zürich

Jobs als Commercial in Lausanne, Vd

Jobs als Finance Manager in Zürich, Zh

Jobs als Medical Director in Zürich, Zh

P2607 - Medical Director, Oncology

Debiopharm -
Lausanne, VD

Direkt bewerben

Details zur Stelle

100% | Pensum: 90-100%

Qualifikationen

Klinische Erfahrung
Master

Vollständige Stellenbeschreibung

At Debiopharm, every step we take is guided by one purpose: improving the lives of people affected by cancer and infectious diseases. As a privately-owned Swiss biopharmaceutical company, we’re driven by science, but above all, by the people behind every treatment — the patients and their families.

Through our unique “development only” model, we bring forward promising therapies and transform them into treatments that can reach those who need them most, faster.

Are you ready to lead the charge in developing next-generation cancer therapies? Debiopharm International SA is looking for a visionary Medical Director, Oncology to serve as the clinical architect for our global oncology programs. In this high-impact role, you will lead the clinical strategy and end-to-end development of innovative compounds, bridging the gap between early discovery and transformative patient care. If you are a physician-leader driven by scientific curiosity and the desire to redefine the treatment landscape for solid tumors, we want to hear from you.

Medical Director, Oncology

Location: Lausanne, Switzerland

Department: Clinical Development

Contract: permanent role, full-time.

Executive Summary

As a Medical Director, Oncology, you will serve as the visionary clinical leader for the global development of transformative compounds. You will design and execute end-to-end clinical strategies—from First-in-Human through Phase 2—to address critical unmet medical needs and achieve Debiopharm’s overarching business objectives.

Key Responsibilities

Strategic Leadership: Develop and lead the global clinical strategy for assigned oncology programs, accounting for medical practice trends and the competitive landscape.
Clinical Deliverables: Provide medical input for all key documents, including study protocols, Investigator Brochures, and regulatory registration dossiers.
Program Execution: Deliver the Clinical Development Plan (CDP) in collaboration with study teams, ensuring efficient protocol execution and medical monitoring.
Matrix Collaboration: Drive clinical programs in partnership with Project Management, Clinical Operations, Biostatistics, and Regulatory Affairs to meet decision milestones.
Decision Support: Generate scenarios and risk-management strategies to inform senior leadership and support decision-making.
Network Building: Develop and maintain a global network of Key Opinion Leaders (KOLs), investigators, and patient advocacy groups.
Stakeholder Interaction: Represent the clinical program before regulatory authorities, data monitoring boards, and internal decision boards.
Business Support: Provide medical expertise to support in-/out-licensing activities and market access strategies.

Requirements

Profile Required

Medical Credentials: Medical Doctor (MD) with significant clinical experience in oncology, specifically in solid tumors.
Industry Experience: At least 2 to 5 years of proven success in early-stage oncology drug development (FIH to Phase 2) within the pharmaceutical industry.
Specialized Expertise: Experience in antibody-drug conjugates (ADCs) or radio-oncology is highly preferred.
Leadership Track Record: Demonstrated ability to lead at least one oncology development program through early stages within a matrix organization.
Strategic Mindset: Proven strategic thinker with an innovative mindset, capable of managing uncertainty and driving decisive risk-based actions.
Technical Mastery: Thorough knowledge of GCP, clinical trial design, statistical methodology, and global regulatory development processes.
Collaborative Spirit: Strong ability to establish scientific partnerships with external stakeholders and internal cross-functional teams.
Agile Mindset: Entrepreneurial and autonomous approach, combined with high medical curiosity and a commitment to staying current with scientific progress.

Benefits

What we Offer

Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day
Partner with teams across disciplines, at the forefront of oncology and anti-infective development
An inclusive and respectful workplace — proud to be Equal-Pay certified
Grow in a culture that values people, purpose, and performance
A chance to grow, share, and shape the future of healthcare

What to Expect in the Recruitment Process

If your application is selected, you’ll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams, followed by a panel interview and reference checks. Communication is handled via Workable—check your spam folder for emails from *@outbound.workable.com.

Please contact our HR Department prior to submitting any profiles. We cannot accept unsolicited applications from agencies or recruiters.

Direkt bewerben

Erweiterte Suche

p2607 medical director, oncology Jobs in lausanne vd

P2607 - Medical Director, Oncology

Medical Director, Oncology

Senior Medical Director, Global Risk Management & Safety Surveillance

Director Group Patents

P2614 - Pharmaceutical Quality (pQM) Specialist

Global Early Commercial Manager, Oncology

P2606 - Global Early Commercial Manager, Oncology

P2613 - CSV Lead

Product Manager - Spatial Biology

EHS Expert - All Genders

Principal Clinical Pharmacologist

P2611 - Senior Legal Counsel - Commercial & Privacy

P2609 - Senior Trial Master File (TMF) Specialist

P2604 - Principal Clinical Pharmacologist

Internship - Automatic Document Extraction (m/f/d)

P2618 - Global Value & Access Lead

Internship: Autonomous Downstream Purification for Monoclonal Antibodies (m/fd)

Internship - Microbiology Quality Control (m/f/d)

Project Scheduler/Steerer (CDM 18 months) - All Genders

P2612 - Senior Manager Statistical Programming

Ich möchte aktuelle Job-E-Mails für Stellen als p2607 medical director, oncology in lausanne vd erhalten

Weitere Job-Standorte erkunden

Tools für Jobsuchende

Arbeitgebertools

Durchsuchen

Bleiben Sie in Kontakt