HDV Medical Science Liaison: Pre-Launch Territory Lead

IQVIA

Chicago (IL)

On-site

USD 180,000 - 220,000

Full time

10 days ago
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Job summary

IQVIA is seeking a Medical Science Liaison (MSL) to advance pre-launch medical readiness for hepatitis delta virus (HDV) across the US Central territory. You will map centers, build peer relationships with healthcare professionals, and develop insights for future launch readiness.

The role requires an advanced clinical degree, prior MSL experience, and ability to travel up to 70%. You will engage beyond trial sites to inform decision-making and support trials with compliant scientific

Qualifications

  • Requires advanced clinical, medical, or scientific degree (PharmD/MD/PhD or relevant master’s).
  • Prior MSL experience is required.
  • Demonstrated experience in credible, compliant peer‑to‑peer scientific exchange with HCPs/KOLs.
  • Ability to travel up to 70% within US Central territory.

Responsibilities

  • Advance pre-launch medical readiness for HDV across the US Central territory.
  • Identify key centers, map referral pathways, and build credible peer relationships.
  • Provide compliant scientific dialogue and education with clinicians and investigators.
  • Collaborate with Medical Affairs and Clinical Operations to support trial activities as appropriate.
  • Maintain accurate documentation of engagements in approved systems.
  • Participate in congresses, meetings, and advisory boards as needed.

Skills

MSL experience
Strong communication
KOL mapping
Territory planning
Scientific exchange

Education

Advanced degree (PharmD/MD/PhD)

Tools

CRM systems
Power BI
MS Teams/SharePoint

Job description

IQVIA is seeking a Medical Science Liaison (MSL) to advance pre-launch medical readiness for hepatitis delta virus (HDV) across the US Central territory. You will map centers, build peer relationships with healthcare professionals, and develop insights for future launch readiness.

The role requires an advanced clinical degree, prior MSL experience, and ability to travel up to 70%. You will engage beyond trial sites to inform decision-making and support trials with compliant scientific

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