Job Title: Medical Director - Rare Disease Bio-pharmaceutical
Location: Tokyo, Japan
Company Overview:
Our client s a pioneering bio-pharmaceutical company dedicated to advancing innovative therapies for rare diseases. Committed to making a positive impact on the lives of patients with unmet medical needs, we are seeking a highly qualified and motivated Medical Director to lead our medical affairs initiatives in Tokyo.
Position Summary:
As the Medical Director for Rare Diseases, you will play a critical role in shaping and implementing the medical strategy for our rare disease portfolio. This leadership position requires a seasoned medical professional with a deep understanding of rare diseases, strong strategic thinking, and a commitment to advancing the science and practice of medicine.
Key Responsibilities:
Medical Strategy and Leadership:
Develop and execute the medical affairs strategy for rare disease programs in alignment with corporate goals.
Provide medical leadership and guidance to cross-functional teams, ensuring the integration of medical insights into all aspects of the business.
KOL Engagement and Scientific Communication:
Cultivate and maintain strong relationships with key opinion leaders (KOLs) and medical experts in the field of rare diseases.
Lead the development and execution of scientific communication plans, including publications, medical education, and advisory boards.
Clinical Development Support:
Collaborate closely with the clinical development team to provide medical input into study design, protocol development, and data interpretation.
Review and contribute to regulatory documents, including Investigator Brochures and clinical study reports.
Medical Information and Training:
Oversee the provision of accurate and timely medical information to healthcare professionals, patients, and internal stakeholders.
Develop and deliver medical training programs for internal teams to ensure a deep understanding of rare diseases and our therapeutic portfolio.
Regulatory Compliance:
Stay informed about relevant medical and regulatory developments, ensuring compliance with local and global regulations.
Collaborate with regulatory affairs to contribute to the preparation and submission of regulatory documents.
Qualifications:
Medical Doctor (MD) degree or equivalent, with specialization in a relevant therapeutic area.
Minimum of 10 years of experience in medical affairs within the bio-pharmaceutical industry, with a focus on rare diseases.
Strong understanding of the Japanese regulatory environment and experience with regulatory interactions.
Proven ability to engage with key opinion leaders and build collaborative relationships.
Excellent communication skills and the ability to convey complex medical concepts to diverse audiences.
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