Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.
Purpose & Scope of Position:
This role will provide strategic guidance to shape and execute local medical strategies in alignment with the Solta Global and APAC organization’s strategic goals. This role will be responsible for developing & nurturing relationships with internal & external stakeholders, playing a key role in guiding innovation pipelines and medical communications based on R&D and Solta strategic priorities in South Korea.
This role will report to the APAC Medical Manager.
Job Responsibilities:
- Customize and implement local medical strategic plans aligned with R&D and regulatory objectives; oversee execution progress and outcomes to ensure timely and targeted delivery.
- Provide scientific leadership in cross-functional collaboration by contributing medical insights, supporting technology application, and fostering KOL engagement.
- Represent the medical function at the local Promotional Review Committee, ensuring alignment with compliance standards and local regulatory requirements.
- Drive medical education and insight integration by leading educational initiatives, engaging KOLs, and collecting clinical insights to inform R&D and strengthen scientific communications.
- Coordinate stakeholder engagement by representing Solta’s medical programs internally and externally, aligning strategies across KOLs, advisory boards, investigators, and CROs.
- Lead regional medical strategy by managing medical education and communication programs in South Korea, ensuring compliance, timely execution, and data generation to support product competitiveness.
- Support pre-registrational and post-marketing studies, accelerating patient enrollment while maintaining compliance with regulatory and SOP standards to advance research and pipeline development.
- Provide clinical expertise in the preparation and review of medical device submission materials for South Korea’s MFDS, ensuring regulatory compliance and facilitating efficient approval processes.
Requirements for Position
Advanced Degree: A Master’s degree or higher is required; an MD, PharmD, or PhD is preferred.
Industry Experience: 3–5 years of experience in medical affairs within the aesthetic medical device industry, with a preference for experience in energy-based devices.
KOL Engagement: Proven success in outreach and relationship-building with Key Opinion Leaders.
Evidence Planning: Demonstrated experience in developing and executing integrated evidence plans, including scientific communications.
Medical Communications: Proficient in leading medical communication and education strategies.
Regulatory Knowledge: Solid understanding of the medical device industry, including familiarity with South Korea’s medical device regulations.
Data Analysis: Strong skills in data analysis and interpretation, with a proven track record in this area.
Publications: A publication record that reflects experience in disseminating research findings is preferred.
Business Acumen: Ability to thrive in a fast-paced, entrepreneurial, and dynamic environment, with strong business acumen.
We are an Equal Opportunity Employer. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.