Medical Scientific Liaison – Oncology /Cluj

About this role

Responsibilities

• Work in a cross-functional brand team as a medical-scientific expert in the therapeutic area
• Development of solid Field Engagement Plans and x-functional Account Management plans
• Work closely with Regulatory, Market Access, and Marketing and other functions on field related medical issues and help support the oncology compounds during the entire lifecycle.
• Support local, regional and global AstraZeneca clinical research program and externally sponsored research projects.
• Help create meaningful real-world evidence data generation projects in collaboration with the brand team across the lifecycle of the brands in your therapeutic areas.
• Provide medical-scientific input on our sales promotion and other activities, including their implementation and potentially the material used.
• Help set up and provide medical-scientific training and further education in your therapeutic area for the sales force and other AZ personnel.
• Organization and execution of scientific events such as symposia, other educational initiatives for healthcare professionals
• Organization of and participation in (regional) advisory board meetings
• Build and maintain expertise in your therapeutic area by continuous education and by participation in national and international congresses and AstraZeneca events.
• Support of the Medical Governance-Team (Medical Information / Patient Safety) in handling of external medical and scientific requests
• Ensure compliance with all local regulatory requirements and AstraZeneca Local and Global Policies and Guidelines

Requirements

• University degree in a health-related or bio-sciences field
• Good understanding of the execution of field medical affairs plans, previous knowledge and expertise in oncology and/or haemato-oncology is a strong plus.
• Professional experience of working in the pharmaceutical industry, preferentially as MSL or within Medical Affairs in one of the therapeutic areas mentioned above; experience within Clinical research will also be considered.
• Thorough knowledge of the local regulatory and market access requirements related to medical affairs activities.
• Comprehensive knowledge of the legal and ethical framework and the procedural guidelines that apply to the promotion and approval of medicinal products in Romania.
• Quick self-learner, ability, and willingness to work in a team and independently.
• Communicative competence and presentation skills
• Very good command of written and spoken English and Fluent Romanian
• High-level of scientific knowledge and ability to analyse and process clinical and scientific data.
• Experience in liaising with healthcare professionals
• Exceptional written and verbal communication skills, including communicating complex technical, scientific, or medical information to broad audience types.
• Driving license