AML Medical Science Liaison — Southeast Territory

IQVIA

Atlanta (GA)

On-site

USD 170,000 - 210,000

Full time

3 days ago
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Job summary

IQVIA seeks experienced Medical Science Liaisons to support a late-stage AML program. The role centers on field-based scientific exchange with investigators and hematology/oncology clinicians to discuss MRD, relapse risk, and evolving care standards.

As an MSL, you will engage KOLs, support investigator meetings, summarize data for medical audiences, and travel extensively across the territory, while adhering to compliance and governance requirements.

Qualifications

  • Advanced degree in a scientific or clinical field.
  • Minimum 4 years of MSL or equivalent experience in hematology/oncology.
  • Willingness and ability to travel up to 70% across assigned territory.

Responsibilities

  • Develop and maintain scientific relationships with KOLs and investigators across the territory.
  • Engage in compliant, peer-to-peer scientific discussions on AML, hematologic malignancies and biomarkers.
  • Support disease-state education, advisory boards, and investigator meetings in accordance with compliance requirements.
  • Communicate complex clinical data clearly to diverse external stakeholders including physicians and researchers.
  • Capture field insights and communicate actionable intelligence to inform Medical Affairs and launch readiness.
  • Maintain current knowledge of literature, congress data, trial designs, endpoints, and emerging therapies.

Skills

MSL experience
Scientific communication
Travel readiness
KOL engagement
CRM proficiency
Oncology knowledge

Education

Advanced clinical or scientific degree

Tools

CRM platforms
Microsoft Office
Microsoft Teams

Job description

IQVIA seeks experienced Medical Science Liaisons to support a late-stage AML program. The role centers on field-based scientific exchange with investigators and hematology/oncology clinicians to discuss MRD, relapse risk, and evolving care standards.

As an MSL, you will engage KOLs, support investigator meetings, summarize data for medical audiences, and travel extensively across the territory, while adhering to compliance and governance requirements.

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