pPhilogen is a Swiss–Italian integrated biotechnology company founded in 1996, focused on the development of innovative biopharmaceuticals for cancer therapy and inflammatory diseases ( /p h3Your Role /h3 pWe are seeking a highly motivated and experienced bMedical Director /b to join our Clinical Department, reporting directly to Philogen's Chief Medical Officer (CMO). /p pYou will play a key role in providing medical oversight, expertise, and leadership to ensure the strategic planning, development, and implementation of clinical trials, collaborating closely with the RD Department to ensure excellence in clinical trial execution in the best interests of patients. /p h3Key Responsibilities /h3 ul liProvide support in developing strategic plans for the company's product portfolio to ensure the success of development programs. /li liWork cross-functionally, providing medical insights, to define, plan and implement Phase 1-3 clinical studies through clinical proof of concept to support the development of new compound and new indications. /li liEnsure compliance in all medical activities as per Philogen’s SOPs and local regulations. /li liDevelop and mantain scientific relations with leading physicians to consult on various topics including Clinical Advisory Boards. /li liDevelop processes and procedures to ensure the safety and monitoring of our products including processes to address product issues, recalls and product complaints. /li liManage medical/clinical supervision/oversight of individual clinical trials. /li liProvide medical input into complaint and adverse event investigations.



/li liInterface with physicians and/or patients related to medical inquiries associated with our products /li liSupport the business development resource to increase the Company’s position and reputationin the marketplace. /li liCollaborate with opinion-leaders and professional faculty to best design and implement projects. /li liEnsure drug safety and surveillance activities are consistent with established regulations and internal SOPs to meet or exceed safety objectives. /li liProvide support in monitoring efficacy trends by reviewing clinical data (i.e. evaluation of inclusion criteria and protocol deviations). /li liInteract with regulatory agencies and clinical centers in order to support the Company’s development program. /li liParticipate in Strategy Meetings. /li liProvides medical expertise in all regulatory, early access and reimbursement approval processes. Ensure content and quality of the Clinical Part of the Submission Dossier. /li liAttend and present materials, as needed, at meetings with Company as well as extra-company meetings. /li liPrepare and present scientific articles and posters at international conferences. /li /ul h3Who We Are Looking For /h3 pEducational Requirements: A degree in Medicine (M.D.) is mandatory,



preferably with an additional track record in Oncology. /p pRequired Experience: A minimum of 5 years of experience in a similar position within a pharmaceutical company. /p pLanguage Skills: An excellent command of English, both written and spoken. /p pLeadership and Collaboration: Demonstrated ability to build trust and confidence across teams and departments. /p pInterpersonal and Organizational Skills: Excellent interpersonal, managerial, and organizational capabilities. /p pCommunication Skills: Strong scientific writing and presentation skills. /p pProfessional Approach: Ability to work independently and efficiently, with strong attention to detail and a commitment to meeting deadlines. /p h3What We Offer /h3 pWe offer employment under the applicable Italian National Collective Bargaining Agreement (CCNL) for Industrial Executives (Dirigenti Industria) and a competitive compensation package with a base gross annual salary starting from €120,000. /p pThe final compensation package will be determined based on objective and neutral criteria, taking into account the candidate's experience, qualifications, seniority, and level of responsibility, as assessed throughout the selection process. /p h3Job Location /h3 pMilan or Siena /p pwe welcome applications from candidates of any gender orientation or expression, sexual orientation, age, ethnicity, or religious belief. /p pIn compliance with Directive (EU) 2023/970 and Italian Legislative Decree No. 96 of 7 May 2026, this job advertisement has been drafted using gender-neutral criteria. /p #J-18808-Ljbffr

📌 Medical Director (Milano)
🏢 Philogen
📍 Milano