Senior Manager, Scientific Affairs APAC

Apply through My Career Navigator attaching an updated CV Evidence planning Work cross functionally with Global Clinical, APAC, HEMA, Marketing, and others to identify scientific/clinical evidence needs in APAC Ensure Evidence needs are integrated into APAC Evidence plans Evaluate external clinical research proposals and collaborate with Clinical and Scientific Affairs, HEMA, and APAC marketing groups to advise on how these research proposals fit into an overall clinical strategy Serve on the Corporate ISR Committee to ensure APAC evidence strategies are being considered during the evaluation of Corporate ISR applications Establish and maintain relationships with Key Opinion Leaders (KOLs) in respective therapeutic areas to establish a strong scientific presence in the practicing and academic communities Develop data dissemination plans internally and externally according to data release and strategic business priorities Ensure data are scientifically accurate and relevant Work with customers to identify and evaluate podium presentation and publication opportunities and ensure clinical and strategic relevance. Ensure speaker readiness through training and consistent messaging. Demonstrates deep expertise in the clinical science and evidence base supporting the company's product portfolio and drives the continuous gathering and development of data intelligence within the therapeutic area. Support internal educational efforts as a therapy and scientific expert to the commercial organization. Strongly collaborate with APAC Marketing, HEMA, & Medical Education, as well as Global Clinical & Scientific Affairs, and APAC Medical Affairs to ensure alignment and buy in. Acts as a key liaison between commercial and scientific functions, ensuring that all external and internal communications are grounded in robust clinical and scientific evidence. Represents APAC Scientific Affairs at the Global Clinical leadership level, contributing regional insights, scientific perspectives, and unmet clinical needs to inform global strategy and evidence planning. Upholds the integrity and compliance of all scientific activities, ensuring alignment with company standards, ethical principles, and relevant regulatory and industry codes Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field (advanced degree preferred: MD, PhD, PharmD). 8 - 10 years of experience related to healthcare of which minimum 5+ years of experience in Medical Affairs within the pharmaceutical, biotechnology, or medical device industry. Strong understanding of clinical research, medical strategy development, and regulatory landscapes. Experience in scientific exchange with KOLs and external stakeholders. Demonstrated ability to provide strategic medical input and review scientific content for promotional and non-promotional use. Proven experience partnering with Marketing, Regulatory, Clinical, and Commercial teams to achieve business and scientific objectives. Excellent written and verbal communication skills; strong command of English proficiency is required to drive communication and write posts (English) to share updates and news on medical and scientific breakthroughs) and research abilities. Ability and willingness to travel within the region (up to 30%)