Global Medical Affairs Manager

Overview
The Global Medical Affairs Manager is part of the Medical Affairs Team and represents the nexus of cutting-edge

medical and scientific insights with internal and external stakeholders contributing to drive medical innovation in

the therapeutic areas of competence and throughout the entire product life cycle.

Reporting to the Global Medical Affairs Lead, he/she is in charge for active and value-adding scientific

contributions to cross-functional teams internally and engagement with key external stakeholders

Main Activities & Responsibilities
Serve as the primary scientific and medical expert for the assigned therapeutic area/products

with internal and external stakeholders.

Participate as representative of Global Medical Affairs in Global Project Teams/ Global Brand

Team.

Contribute to the development and execution of the Global Medical Affairs Plan according to

strategic company milestones and budget.

Work closely with internal stakeholders to execute that all activities in the Medical Affairs plan

designed to meet shared objectives are implemented and performed in a timely manner.

Contribute to marketing strategies with scientific input and collaborate on organizing medical

events.

Provide impactful feedback/information to internal stakeholders on emerging clinical and

scientific trends from external interactions to help shape company research and to ensure the

safe and appropriate use of Menarini Group products.

Build specific excellence and integrity within the healthcare community. Develop contacts with

key clinicians, patient's association and other medical/scientific groups.

Contribute to Mapping of Key Opinion Leaders (KOLs) on the disease and KOLs insights on the

product.

Analyze, synthesize, and present medical scientific information in a structured way.

Prepare and deliver training sessions on therapeutic areas and assigned products.

Assist in the development and execution of clinically relevant medical meetings (e.g., advisory

boards, consultancy and investigator meetings), as requested.

Contribute to planning, coordination, and presentations at global and national advisory boards

and other meetings.

Contribute to publication planning, delivery, and dissemination

Contribute to the development and implementation of key international congresses

Develop, review and approve responses to unsolicited requests for medical information in line

with company's SOPs and code of practice.

Develops, review and approve promotional and educational materials for the allocated

therapeutic area.

Act as Study Medical Expert in the development of studies from initiation until publication and

evaluate initiated investigator studies in the correspondent therapeutic area.

Interact with key medical societies

Support and review of grants for scientific projects in collaboration with clinical operations

Provides support and input into regulatory authority interactions, for example RMPs, PSURs,

defending risk/benefit, Product Information.

Provides support and input into early phase or market access aspects of clinical development

plans.

Contribute to developing SOPs and Working Instructions to improve efficiency, quality and

compliance in processes.

Coordinate approval of contracts for external (consultancy/speaker) activities with HCPs or other

third parties.

Collaborate with external providers in different activities according to the Menarini Group

code of practice and policies.

Ensure all medical projects, materials and presentations are compliant to pharmaceutical codes.

Act within compliance and legal requirements as well as within company guidelines.

Other duties as assigned

Job Requirements
Education (Medical Doctor Degree)

• Years of experience (≥2 )
• Language skills and level of proficiency (Business fluency in English, both spoken and written)
• Other skills:
• Good verbal and written communication skills.
• Strong organizational, and cross-functional collaboration skills.
• Driven by Learning & Personal Development
• Ability to effectively collaborate in a dynamic and global environment.