P2620 - Oncology Safety Physician

• 30 juin 2026 • Indefinite duration • Lausanne For our Clinical Safety and Pharmacovigilance team within the Research and Development department based in Lausanne, we are looking for a :   Oncology Safety Physician ### 100 %, permanent contract, at the Lausanne headquarters.   In this role, you will be responsible for the active management and risk assessment associated with products under development in oncology as well as antibiotics under the responsibility of the Head of Clinical Safety and Pharmacovigilance. You will also support the deployment of early phases in healthy volunteers in collaboration with the Clinical Pharmacology & Drug Metabolism team.   Your responsibilities will include, but are not limited to: • Evaluate and establish the safety profile of this product in collaboration with various company experts and/or external partners • Provide medical advice regarding the safety aspects of : • documents intended to be submitted as part of an accelerated approval procedure, preparation of investigator brochures, development safety update reports • Be responsible for safety monitoring activities for this product, including medical review of individual safety cases directly in the safety database and signal detection activities (continuous review of safety data) • Ensure supervision of outsourced medical activities with our pharmacovigilance service provider • Develop and lead, in collaboration with the relevant functions in clinical medicine, biometry and clinical pharmacology, the implementation of a signal detection tool. • Be a member of study teams and work collaboratively and proactively in a matrix environment. • Participate in IDMC meetings or other safety-related interactions with external collaborators, as well as internal safety working groups Your profile · Doctor of medicine, with experience in clinical safety in the early clinical phases of drug development within a global pharmaceutical company or a global CRO · At least 5 years of direct experience in the Biotech/Pharmaceutical industry in clinical safety · First experience in drug development in oncology, in early phases, an asset · Excellent leadership, management, collaboration, communication and decision-making skills · Ability to effectively prioritize activities and meet multiple deadlines with attention to detail, setting high-performance standards for quality · Proficiency in the Microsoft 365 suite, an appetite for digital tools is a plus · Excellent written and oral communication skills in English, French is an asset Debiopharm offers its employees : · An international, very dynamic environment with a long-term vision. · Cross-functional collaboration at the cutting edge of the most advanced scientific developments in oncology and in the antibacterial industry · Exposure to a wide variety of fields and functions within clinical development and the pharmaceutical industry · Participation in a company where innovation, people and entrepreneurship are the fundamental keys to success. · Proud to be certified Equal Pay, we guarantee all our employees the same opportunities *The use of external recruitment agencies or headhunters requires prior approval from our Human Resources department. Debiopharm's Human Resources department requests that external agencies or recruiters do not directly contact Debiopharm employees or members of the Board of Directors for the purpose of presenting candidates.* *The submission of unsolicited CVs before an agreement between the Human Resources department and the external agency or recruiter creates no implied obligation on the part of Debiopharm.* *Debiopharm will not accept unsolicited CVs from sources other than the candidates themselves for current or future positions.*