About this role
Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible and specialized medical and commercial services. In this Medical Science Liaison role, support activities across Medical Affairs and Clinical Development objectives for pipeline products in rare disease. Serve as a key interface with clinical trial sites and collaborate with Medical Affairs to engage key opinion leaders.
Build enduring relationships with HCPs, patient advocacy groups, professional societies, and institutions. Serve as primary interface between client and clinical trial sites across development programs, working closely with Clinical Development and Clinical Operations. Advise and participate in planning and set-up of clinical studies while representing client at scientific congresses.
Business Unit is Medical Affairs, reporting to Program Director. Home-based in Singapore or South Korea covering APAC territory including Australia, Japan, China, Singapore, South Korea with 50-70% travel. Individual contributor role in a team using EPIIC values: excellence, passion, integrity, innovation, collaboration.
Amplity offers remote working with flexible hours focused on outputs for work-life balance. Hands-on learning tailored to expertise with career growth opportunities. Diverse, equitable, inclusive environment supporting holistic wellbeing and global presence.
Requirements
- Advanced degree in medicine, pharmacy, or life sciences
- Deep therapeutic expertise in oncology or rare diseases
- Experience interfacing with clinical trial sites and clinical operations
- Proven track record engaging key opinion leaders and HCPs
- Knowledge of Medical Affairs and Clinical Development processes
- Ability to travel 50-70% across APAC territory
- Strong scientific communication skills for non-promotional exchange
Responsibilities
- Build and develop enduring relationships with HCPs, patient advocacy groups, professional societies, and institutions
- Create constructive cross-functional partnerships with internal and external stakeholders
- Serve as primary interface between client and clinical trial sites across all development programs
- Work closely with Clinical Development and Clinical Operations
- Advise and participate in the planning and set-up of clinical studies
- Represent client at select scientific congresses and professional society meetings
- Share important clinical and scientific insights gathered from fieldwork to cross-functional teams
- Identify and engage key opinion leaders to communicate non-promotional scientific and medical information
Benefits
- Car allowance, annual performance-related bonus up to 15%, medical coverage or contribution
- Remote working with flexible hours focused on outputs
- Hands-on learning tailored to needs and expertise
- Opportunity to impact breakthrough medicine from day one
- Diverse, equitable, inclusive environment where every voice is heard
- Support for holistic wellbeing approach
- Global presence with cross-functional partnerships
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