Detail Pekerjaan

Perusahaan Favorit

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BD&marketing supv for Medical device: Neuro/ECMO/ life saving product

Ikon terverifikasi

Mitra Premium Pintarnya

Pasar Minggu, Kota Adm. Jakarta Selatan

Bisa dinegosiasikan

Other

, Onsite

Persyaratan Umum

Usia

Semua usia

Pendidikan

Tidak ada minimal pendidikan

Jenis Kelamin

Pria/Wanita

Lokasi

Seluruh Indonesia

Pengalaman

Tanpa pengalaman bekerja

Deskripsi Pekerjaan

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 Major in Pharmacy/Biotechnology/Engineer or related Solid knowledge base on medical device at Neuro/life saving product Understanding business objective Good relationship with KOL Proficient in English Strong ability for literature retrieval Ability to efficiently deliver result under pressure

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