Overview In this Medical Science Liaison role, you will bridge science and clinical practice to support a late-stage AML program. You'll engage investigators and hematology/oncology teams, share clinical and translational data, and capture insights on disease biology, MRD, relapse, and evolving care standards. You'll partner with Medical Affairs to inform strategy and conduct compliant scientific exchanges. The position offers exposure to cutting-edge AML research, investigator-initiated studies, and cross-functional collaboration in a global clinical development context.
Compensation / Benefits- incentive plans
- bonuses
- health and welfare benefits
Responsibilities- Build and maintain scientific relationships with KOLs, investigators, and hematology/oncology centers across the territory
- Conduct compliant, peer-to-peer scientific discussions on AML, biomarkers, MRD, relapse risk, and evolving standards of care
- Communicate complex clinical data clearly to diverse external audiences
- Support disease-state and scientific education programs, advisory boards, and investigator meetings within compliance requirements
- Execute scientific exchange with HCPs, formulary committees, and other stakeholders using approved materials
- Identify and communicate training needs in the medical community
- Serve as a contact for initiation of investigator-initiated studies and provide study development support
- Monitor and capture field insights to shape research, development, and launch strategies
- Maintain clinical expertise through conferences, journals, and continuous education
- Increase visibility with thought leaders and enhance interactions between the client company and industry experts
- Collaborate with Medical Affairs leadership to execute the field medical plan and document interactions in CRM systems
- Maintain high standards of scientific integrity, ethics, and compliance
Key requirements- Advanced clinical or scientific degree required; PharmD, MD, DO, PhD, DNP, NP, PA or equivalent strongly preferred
- Minimum 4 years of MSL or relevant clinical experience in hematology/oncology
- Minimum 3 years of experience in hematology/oncology with demonstrated therapeutic area expertise
- Proven ability to communicate complex scientific information to diverse audiences
- Strong understanding of oncology treatment landscapes and market dynamics
- Proficiency with CRM platforms, Microsoft Office Suite, Microsoft Teams, and other digital engagement tools
- Ability to work independently and with cross-functional teams
- Knowledge of clinical trial processes, FDA regulations and OIG guidelines
- Valid driver's license and willingness to travel up to 70%
- Familiarity with investigator-initiated studies, registries, and observational research
- Excellent verbal and written communication
- Cross-functional collaboration
- Stakeholder engagement and relationship building
- CRM platforms
- Microsoft Office Suite
- Microsoft Teams
