Global Medical Affairs Manager

Tipo Contratto: Da definire

Overview :

Global Medical Affairs Manager Part of the Medical Affairs Team, representing the nexus of cutting-edge medical and scientific insights with internal and external stakeholders, contributing to medical innovation across therapeutic areas and throughout the product lifecycle. Reports to the Global Medical Affairs Lead. Responsible for active scientific contributions to cross-functional teams and engagement with key external stakeholders. Reports to: Global Medical Affairs amp; Clinical Operations Director

Contract : Temporary (12 months).

Main Activities amp; Responsibilities :

Serve as the primary scientific and medical expert for the assigned therapeutic area/products, engaging with internal and external stakeholders. Participate as a representative of Global Medical Affairs in Global Project Teams and Global Brand Teams. Contribute to developing and executing the Global Medical Affairs Plan and Menarini Marketing Multichannel Model (M4) aligned with strategic milestones and budget. Collaborate with internal teams to ensure timely implementation of activities in the Medical Affairs Plan and M4. Provide scientific input to marketing strategies and assist in organizing medical events. Share insights on emerging clinical and scientific trends from external interactions to inform company research and ensure safe, appropriate use of products. Build relationships with healthcare professionals, patient organizations, and scientific groups; develop KOL mapping and insights. Analyze and present medical scientific information clearly and effectively. Prepare and deliver training on therapeutic areas and products. Assist in planning and executing medical meetings such as advisory boards and investigator meetings. Contribute to publication planning, presentation, and dissemination. Support development and implementation of international congresses. Respond to unsolicited medical information requests in line with SO Ps and codes of practice. Review and approve promotional and educational materials. Act as Study Medical Expert in clinical studies, from initiation to publication. Engage with medical societies and support scientific grants. Support regulatory interactions, including RM Ps, PSU Rs, and product information. Contribute to clinical development plans, SO Ps, and working instructions. Coordinate external contracts and collaborate with external providers following company policies. Ensure compliance of all medical projects and materials with pharmaceutical codes and legal requirements.

Job Requirements :

Medical Doctor Degree Fluent in English, both spoken and written Excellent communication skills Strong organizational and cross-functional collaboration skills Motivated by learning and personal development Ability to work effectively in a dynamic, global environment Deep understanding of disease states, treatment algorithms, and experience in relevant therapeutic areas Knowledge of promotional regulations, safety reporting, and regional health policies Ability to lead training initiatives and best practices
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