Medical Lead Hemato-oncology

1 mese fa

Roma, Italia ABBVIE A tempo pieno

Set up and lead a Medical Affairs team. Provide leadership, strategic direction and mentorship to direct reports, as appropriate, and fulfill line management responsibilities accordingly
- Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) within Hemato-Oncology through participation at key internal meetings, relevant congresses, and seminars and by regular self-study of the literature.
- Provide expert medical/scientific advice for assigned products and related therapeutic areas in Hemato-Oncology cross-functional teams, including responding to requests for scientific information; contribute to the development and medical and scientific accuracy of core dossiers generated/supported by the medical department (i.e. pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).
- Establish and maintain professional and credible relationships with key thought leaders / external experts and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion fora etc.
- Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.
- Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)
- Deliver training to sales forces and other departments; develop and update relevant training materials.
- Clinical Research Activities: Design and implement clinical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies). Provide the required oversight to manage review, approval and conduct of IIS studies.
- Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).
- Review promotional material. Ensure the medical/scientific content is correct and fully compliant with AbbVie’s internal policies and guidelines.
- Provide medical/scientific input into marketing strategy and key commercial initiatives, as required. Monitor the environment for competitive intelligence (e.g. product strategies, studies, commercial messages, positioning, etc.) and communicate, where appropriate, within the Company.
- Development and execution of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans. Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures and accepted standards of best practice.
- Medical Degree or Bachelor’s degree in a scientific discipline or higher.
- Working experience of >5 years in pharmaceutical industry. General knowledge on drug development and clinical research is an advantage. Experience with Hemato-Oncology and an existing network is a plus.
- Keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and in medical research in general.
- Excellent written and spoken communication and presentation skills.
- Fluency in written and oral English is highly desirable in order to facilitate communications between the affiliate medical department, Global and Area Medical Affairs and other AbbVie functional staff.
- High customer orientation. Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.
- Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large. Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage. Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate’s medical and clinical activities as necessary.
- Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.

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