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IQVIA is seeking a scientifically credible and field-based Medical Science Liaison (MSL) to support a high-impact oncology clinical trial across Central and Eastern Europe. You’ll serve as a key scientific resource to clinical trial sites—building strong relationships with investigators, supporting site activation and enrollment, and facilitating high-quality scientific exchange.

Location: Field-based – Germany 

Territory: Germany, Austria, German-speaking Switzerland, Poland, and Czech Republic 

All activities must be conducted in accordance with German and EU regulations, industry codes of practice, and IQVIA’s internal compliance policies.

IQVIA is an equal opportunity employer (m/w/d). We welcome applications from all qualified individuals regardless of gender, background, or identity.

Key Responsibilities:

• Provide field-based medical support to clinical research programs in oncology.
• Deliver credible, balanced presentations on disease area and investigational therapies to investigators and site staff.
• Engage with clinical trial sites to understand and help resolve medical barriers to patient recruitment and screening.
• Collaborate with site management and monitoring teams to support site initiation and engagement.
• Facilitate compliant scientific exchange with healthcare professionals (HCPs) and key opinion leaders (KOLs).
• Capture and report field intelligence, including protocol feedback, treatment landscape insights, and competitor activity.
• Represent the program at scientific meetings, advisory boards, and congresses.
• Maintain up-to-date knowledge of the disease area, investigational assets, and relevant clinical data.
• Ensure all activities are conducted in accordance with applicable laws, regulations, and company policies.

Required Qualifications:

• Advanced scientific degree: MD, PhD, PharmD (strongly preferred).
• Minimum 2 years’ experience as an MSL or in a scientific/medical role.
• Oncology experience is essential, ideally in solid tumors.
• Fluency in both German and English is required for effective communication with local stakeholders and regulatory bodies.
• Proficiency in Polish or Czech is a plus.
• Willingness to travel extensively across the assigned territory.
• Valid driver’s license.

Why This Role Matters:

• Represent a first-in-class therapeutic approach with a dual mechanism of action.
• Influence trial success through strategic site engagement and real-time insights.
• Grow your career in a fast-paced, science-led environment where your expertise matters.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com