Informații principale
Medical Project Manager (m/f/d)
Poziție: Nu este specificat
Start: Îndată ce este posibil
Final: Nu este specificat
Localizare:
Zürich, Elveția
Metoda de colaborare: Doar proiect
Tarif pe oră: 0 Lei
Ultima actualizare: 29 Mai. 2025
Descrierea și cerințele proiectului
Tasks:
• Provide project management leadership for the rare renal therapeutic area
• Project Planning and Execution: Develop comprehensive project plans, define scope, set objectives, and establish timelines. Ensure all projects are delivered on time, within scope and within budget
• Ensure the development and execution of local project plans in support of best clinical practices and overall objectives aligned with Global Medical Affairs
• Stakeholder Management: Manage relationships with internal and external stakeholders, including medical professionals and key opinion leaders. Ensure that stakeholder needs and expectations are met
• Symposium Organization: Plan, coordinate, and execute medical symposiums and conferences to advance knowledge sharing and collaboration within the medical community
• Support external educational activities to promote knowledge sharing and professional development within the medical community
• Lead the organization of advisory boards and other platforms for insight gathering to inform strategy and decisions
• Enable countries to efficiently implement global medical initiatives to ensure consistency and alignment across regions
• Support and advise cross-functional teams to ensure patient-focused activities at all times
• Compliance and Quality Assurance: Ensure that all projects comply with regulatory requirements and organizational quality standards
Requirements:
• Medical (M.D.) or scientific education (Ph.D., Pharm. D.)
• Solid experience in the pharmaceutical industry (Medical Affairs or Clinical Development)
• Previous direct experience with payer interactions, reimbursement applications, and management of early access programs
• Demonstrated ability to accurately and effectively evaluate medical scientific literature
• Knowledge of study design and conduct
• Proven relationship-building skills with key opinion leaders
• Understanding of medical aspects of the therapeutic area along with a willingness to develop in-depth expertise
• Experience working with commercial and market access teams with a strong focus on patient centricity and safety
• Professional level in English, both in oral and written communications
• Excellent user of Office Programs (Word, Excel, PowerPoint)
Advantages:
• Remote work possible
• Renowned company
• Further training opportunities
Duration: 6 MM++