GlaxoSmithKline GmbH & Co. KG
Country Medical Director(m/w/x)
Vollzeitmit HomeofficeManagement
Baar
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
GSGSK
Senior Medical Director, Oncology Clinical Development - Lung(m/w/x)
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Medical oversight for lung cancer clinical trials, guiding study design and safety monitoring. Oncology clinical development experience required. Annual bonus and share-based long-term incentive program.
Deine Match-Analyse
von deinem Karriere-Agenten
Warum dieser Job zu dir passt
Mögliche Lücken
Tipps für deine Bewerbung
Anforderungen
- Medical degree and advanced specialty training in oncology, haematology, or related specialty
- Clinical and pharmaceutical experience in oncology clinical development
- Experience in medical monitoring, safety evaluation, and data interpretation
- Understanding of clinical development, GCP, ICH guidelines, and regulatory frameworks
- Experience operating within cross-functional matrix teams
- Strong scientific communication and stakeholder engagement skills
- Experience contributing to or leading regulatory interactions
- Demonstrated experience engaging with KEEs, advisory boards, and scientific communities
- Track record of scientific publications and congress presentations
- Deep understanding of oncology disease biology and treatment landscape
- Experience mentoring or providing oversight to physicians
- Experience contributing to clinical and technical diligence for business development
- Clinical Data Interpretation
- Clinical Pharmacology
- Clinical Trial Designs
- Clinical Trials Monitoring
- Digital Fluency
- Drug Development
- Drug Regulatory Affairs
- Evidence Based Decision Making
- Executive Presence
- Hematology and Oncology
- Learning Agility
- Matrix Leadership
- Real World Evidence (RWE)
- Scientific Presentations
- Strategic Direction
Aufgaben
- Provide medical oversight and clinical insight across study design, conduct, and data interpretation
- Guide medical monitoring and safety oversight across studies
- Interpret complex clinical and safety data to inform programme-level decisions
- Integrate medical considerations across study execution and programme delivery
- Provide senior medical input into protocol development and study design
- Influence study-level and programme-level decision-making as a senior member of the CMT
- Engage with investigators and Key External Experts (KEEs)
- Represent the programme at advisory boards and scientific forums
- Provide medical guidance and mentorship to Medical Directors
- Guide interpretation of safety data in collaboration with pharmacovigilance
- Participate in safety review forums, providing physician perspective
- Ensure medical monitoring approaches are aligned across studies
- Guide clinical aspects of study design and protocol implementation
- Support resolution of complex medical questions during study conduct
- Ensure consistency of medical considerations across multiple studies
- Interpret complex clinical data across studies to inform programme insights
- Contribute to programme-level data interpretation and benefit–risk assessment
- Guide development of scientific communications, including publications
- Maintain deep understanding of disease biology and treatment paradigms
- Contribute medical expertise to regulatory interactions and Health Authority discussions
- Engage with KEEs and scientific collaborators to support programme development
- Lead or contribute to the clinical and technical diligence assessment of business development opportunities
- Influence cross-functional alignment and programme-level decision-making
- Contribute medical expertise to disease area strategy and evidence planning
- Collaborate across functions to ensure alignment on safety and data interpretation
- Lead or contribute to Oncology Clinical Development-wide initiatives
- Support development of clinical capability within the medical team
- Contribute to talent development and capability building within Oncology Clinical Development
Berufserfahrung
ca. 4 - 6 Jahre
Ausbildung
Bachelor-AbschlussODER
Master-Abschluss
Sprachen
Englisch – verhandlungssicher
Tools & Technologien
GCPICH guidelines
Benefits
Boni & Prämien
- Annual bonus
Attraktive Vergütung
- Share-based long-term incentive program
Gesundheits- & Fitnessangebote
- Health care benefits
Sonstige Vorteile
- Other insurance benefits
- Paid medical leave
Betriebliche Altersvorsorge
- Retirement benefits
Familienfreundlichkeit
- Paid caregiver leave
Großzügige Elternzeit
- Paid parental leave
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens GSK erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Zur Originalanzeige bei GSKÜber das Unternehmen
GS
PharmaceuticalsZug
GSK is a global biopharma company focused on preventing and treating diseases through innovation in specialty medicines and vaccines.
Wie gut ist dein Lebenslauf?
Nejo bewertet ihn, und bringt ihn danach gemeinsam mit dir in Bestform.
Du hast noch keinen Lebenslauf?
Noch nicht perfekt?
- Novocure IncSenior Director, Clinical Regulatory Affairs(m/w/x)Vollzeitmit HomeofficeSeniorBaar
- BridgeBio PharmaSenior Director, Health Economics and Outcomes Research, International(m/w/x)Vollzeitmit HomeofficeSeniorZug
- BridgeBio PharmaSenior Director, Medical Affairs, International(m/w/x)Vollzeitmit HomeofficeSeniorZug
- SobiSenior Medical Materials Coordinator(m/w/x)Vollzeitmit HomeofficeSeniorZug