BD&marketing supv for Medical device: Neuro/ECMO/ life saving product
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Key Responsibilities
• Develop and implement medical affairs strategies and scientific communication plans for assigned products.
• Build and maintain strong relationships with Key Opinion Leaders (KOLs), healthcare professionals, medical societies, and regulatory stakeholders, including organizations such as MOH, BPOM, IDAI, IDI, and other relevant institutions.
• Organize and support medical activities, including advisory board meetings, continuing medical education (CME) programs, scientific symposia, and academic conferences.
• Collect, analyze, and manage medical insights and competitive intelligence, including updates on clinical research, real-world evidence, and treatment landscape developments.
• Develop annual medical action plans and ensure effective execution through close collaboration with internal stakeholders.
• Provide scientific training and medical support to internal teams, distributors, and external partners to ensure accurate and compliant communication of medical information.
• Prepare and update scientific materials, presentations, and training tools for designated products.
• Collaborate closely with Marketing, Sales, Regulatory Affairs, and other cross-functional teams to support business growth and product lifecycle management.
• Support pre-launch medical affairs activities by collecting and summarizing clinical and preclinical data related to pipeline products.
• Work with internal and external Regulatory Affairs teams to support registration activities, including medical evidence collection and preparation/review of English and Bahasa submission documents.
• Manage and supervise external business partners on medical-related activities and projects.
• Act as the responsible person for CDAKB-related requirements and ensure compliance with applicable regulations.
Requirements
Job ID: 153662967
