(Senior) Medical Affairs Manager

About the role

BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeOne , please visit www.beonemedicines.com and follow us on LinkedIn and X (formerly known as Twitter). BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. Job Description: General Description: The (Senior) Medical Affairs Manager will be responsible for medical affairs and governance of the designated therapeutic area and will play a vital role in the design and implementation of a respective Medical Affairs plan to provide the scientific support for marketed products and products in development. Essential Functions of the job: S/he will be responsible for development of medical strategy, plan and tactic in line with global medical strategy and brand strategy. The (Senior) Medical Affairs Manager will also actively contribute to medical input for local investigator-initiated research and global medical and clinical activities with global therapeutic area physicians, including global brand strategy, global clinical trials, brand safety profile discussions, global brand payer dossier. Additional representative responsibilities include, but are not necessarily limited to, the following: Lead the assigned therapeutic area with responsibility for the development of medical strategy development and develop the medical tactics in line with medical strategy to relect local medical/brand's needs. Serve as Scientific leader with local leadership and, as required, managerial support responsibilities for scientific staff such as Medical Science Liaisons (MSL). Liaise and coordinate issues and development of such staff with the Country Medical Director and head of solid tumors and ensure that local needs are addressed. In addition to the generation of scientific data to support medical claims, provide input for the generation of health economic outcome data to support reimbursement. Have responsibility for the provision of input to Research & Development to assist with the lifecycle management of the relevant products, including developing and disseminating appropriate scientific data and ensuring all Medical Affairs activities are conducted with the utmost integrity. Support integration and communication to regulatory and development teams with strategic medical input where appropriate; ensure medical affairs activities are scientifically sound, within relevant guidelines, and of a high standard. Provide input and guidance to medical information and strategy team within the Country to support optimal medical communications and development strategies for the Country. Support to recommend new Country studies, medical affairs activities and investments to Global Medical Affairs leadership Ensure compliance with Country directives for, amongst others, the release of promotional material and medical representative training materials. Together with other members of the Global Medical Affairs team, establish and maintain strong relationships with key opinion leaders for and on behalf of BeOne in all relevant areas to promote the Company's reputation, dedication to patients, and expertise in these areas. Lead and Plan medical tactics as described in below; - Country/Regional Medical and Scientific meeting (i.e., symposium and advisory boards etc) that involve scientific leaders. - Collect, maintain and share the actionable insight with relevant internal stakeholders - Implement EAP (PRAP) or CU (Individual Patient Request)- - Data generation to support medical and brand strategy Support the Investigator Sponsored Trial communication and implemtation. Build reliance with scientific experts via scientific exchange, research, education collaboration as well as interactions with scientific societies and health organization etc Lead the regulatory requirement studies (eg. RMP-PMS and/or registry etc) in collaboration with internal local/global stakeholder and CRO. - Develop the study whole plan including study design and operation plan in collaboration with medical clinical operation manager - Support the development of implemtation plan of the study. - Ensure that the study progress is on-track and fulfill the study outcome according to regulatory requirement. Qualification Requ