Medical Science Liaison – Southeast Region

IQVIA

. Serve as a field-based scientific resource supporting a late-stage AML clinical development program .

Posted 9/19/2026full-timeRaleigh • Florida • United StatesMid-LevelSenior💰 $170,000 - $210,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced clinical expertise in hematology and oncology, with a strong ability to communicate complex scientific information effectively to diverse healthcare stakeholders. Proven experience in medical affairs, clinical development, and executing field medical plans within the oncology landscape.

Highest-signal resume keywords

Advanced Clinical DegreeMedical Science Liaison ExperienceHematology/Oncology ExpertiseCRM ProficiencyClinical Trial Planning

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical DevelopmentScientific EngagementTreatment Guidelines KnowledgeFDA Regulations KnowledgeClinical Research Processes

Soft Skills

Effective CommunicationCollaborationIndependent Work

Tools & Technologies

Microsoft Office SuiteMicrosoft TeamsDigital Engagement Tools

Certifications & Qualifications

PharmDMDDOPhDDNPNPPA

Industry Keywords

AMLHematologic MalignanciesCancer ImmunotherapyBone Marrow TransplantClinical Trial Investigator Relationships

About the role

Key responsibilities & impact

Serve as a field-based scientific resource supporting a late-stage AML clinical development program
Develop and maintain scientific relationships with KOLs, academic investigators, community hematology/oncology leaders, and priority institutions across the assigned territory
Engage in compliant peer-to-peer scientific discussions regarding AML, hematologic malignancies, immunotherapy, mechanisms of action, clinical trial data, biomarkers, MRD, relapse risk, and standards of care
Communicate complex clinical and scientific information to physicians, researchers, advanced practice providers, pharmacists, nurses, and multidisciplinary care teams
Support disease-state education programs, advisory boards, investigator meetings, and other medical activities
Execute scientific exchange with HCPs, KOLs, formulary committees, and other stakeholders using approved materials
Identify medical community training and educational needs
Serve as first point of contact for investigators initiating investigator-initiated studies and provide technical study-development support
Communicate clinical and research issues to MSL leadership to inform research, development, marketing plans, and strategies
Maintain clinical expertise through self-education, conferences, workshops, and journal review
Capture and communicate actionable field insights on unmet needs, clinical practices, treatment barriers, evidence gaps, stakeholder perceptions, patient identification, sequencing, and adoption
Synthesize external insights into strategic recommendations for Medical Affairs, Clinical Development, evidence generation, scientific communications, and launch readiness
Monitor competitive developments, emerging data, clinical trial activity, guidelines, congress intelligence, and investigator interests
Identify and cultivate relationships with clinical trial investigators, research centers, cooperative groups, and institutions
Support scientific discussions related to clinical development programs, trial awareness, and site engagement
Identify clinical research opportunities consistent with company objectives
Partner with Medical Affairs leadership and cross-functional colleagues to execute the field medical plan
Document scientific interactions and insights accurately and timely in CRM or insight management systems
Maintain scientific integrity, ethics, and compliance

Requirements

What you’ll need

Advanced clinical or scientific degree required; PharmD, MD, DO, PhD, DNP, NP, PA or equivalent strongly preferred from an accredited institution
Minimum of 4 years of Medical Science Liaison (MSL) experience or relevant clinical experience within hematology and/or oncology
Minimum 3 years of experience in hematology/oncology required, with demonstrated therapeutic area expertise
Demonstrated track record of success in medical affairs, clinical development, clinical practice, scientific engagement, or related healthcare roles
Strong understanding of healthcare stakeholder segments, treatment landscapes, and market dynamics within oncology
Proven ability to communicate complex scientific and clinical information effectively to diverse audiences
Proficiency with CRM platforms, Microsoft Office Suite, Microsoft Teams, and other digital engagement tools
Ability to work independently while collaborating effectively within cross-functional teams
Compliance with client-specific site access requirements, including applicable vaccination or health screening protocols, may be required
Familiarity with planning and execution of clinical trials in oncology and independent investigator-initiated clinical and/or translational research studies, including registries and observational studies
Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines
Valid driver's license and ability to travel extensively within the assigned territory
Willingness and ability to travel up to 70% of the time
Experience supporting AML, MDS, bone marrow transplant, cellular therapy, cancer immunotherapy, or related hematologic malignancies preferred
Prior product launch experience within oncology or rare disease preferred
Existing strong relationships with academic and community hematology/oncology centers preferred

Benefits

Comp & perks

Health and welfare benefits
Incentive plans, bonuses, and/or other forms of compensation may be offered