AML Medical Science Liaison – Southeast

IQVIA; Atlanta (GA); On-site; USD 170,000 - 210,000; Full time

Job summary

IQVIA seeks experienced Medical Science Liaisons to support a late-stage AML program. This field-based role engages hematologists, oncologists, and investigators to facilitate scientific exchange, discuss data, and capture insights on MRD, relapse risk, and evolving standards of care.

You will build relationships with investigators, support investigator-initiated studies, and work with cross-functional teams to inform medical strategy while adhering to applicable compliance frameworks.

Qualifications

• Advanced clinical or scientific degree required (PharmD/MD/DO/PhD/etc).
• Minimum 4 years MSL experience or relevant clinical experience in hematology/oncology.
• Minimum 3 years hematology/oncology experience with proven therapeutic expertise.
• Strong ability to communicate complex information to diverse audiences.

Responsibilities

• Develop and maintain scientific relationships with investigators, academic centers, and hematology/oncology leaders.
• Engage in peer-to-peer scientific discussions on AML, MRD, relapse risk, and evolving standards of care.
• Communicate complex clinical data clearly to physicians, researchers, and care teams.
• Support disease-state and scientific education programs, advisory boards, and investigator meetings.
• Identify clinical research opportunities and communicate insights to leadership.
• Maintain clinical expertise through conferences, journals, and continuous education.

Skills

MSL experience

Hematology/Oncology knowledge

Scientific communication

CRM platforms

Travel readiness

Cross-functional collaboration

Clinical development knowledge

Education

Advanced clinical or scientific degree (PharmD/MD/PhD/DO/PN/PA)

Tools

CRM platforms

Microsoft Office

Microsoft Teams

Job description

IQVIA seeks experienced Medical Science Liaisons to support a late-stage AML program. This field-based role engages hematologists, oncologists, and investigators to facilitate scientific exchange, discuss data, and capture insights on MRD, relapse risk, and evolving standards of care.

You will build relationships with investigators, support investigator-initiated studies, and work with cross-functional teams to inform medical strategy while adhering to applicable compliance frameworks.