Medical Science Liaison, Hematology

Amplity Health

. Establish and maintain collaborative relationships with researchers, investigators, key opinion leaders, and healthcare stakeholders in hematology and myeloproliferative neoplasms .

Posted 10/9/2026full-timeGermanyMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in hematology and myeloproliferative neoplasms, with a strong ability to build relationships and conduct scientific exchanges with healthcare stakeholders. Proficient in clinical trial design and execution, regulatory compliance, and translating insights into actionable medical strategies.

Highest-signal resume keywords

Medical Affairs ExperienceHematology ExpertiseClinical Trial DesignRegulatory Compliance KnowledgeRelationship Building

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial DesignScientific ExchangeData AnalysisMedical Strategy DevelopmentPipeline Asset Knowledge

Soft Skills

Networking SkillsStrong Communication SkillsTeam CollaborationIndependent FunctioningPresentation Skills

Certifications & Qualifications

Advanced Doctoral Degree (MD, PhD, PharmD) or MSc

Industry Keywords

HematologyMyeloproliferative NeoplasmsHealthcare SystemsRegulatory GuidelinesBiotech Experience

About the role

Key responsibilities & impact

Establish and maintain collaborative relationships with researchers, investigators, key opinion leaders, and healthcare stakeholders in hematology and myeloproliferative neoplasms
Conduct compliant, high-quality scientific exchange on disease education, emerging science, and investigational therapies
Build relationships with academic centers, research institutions, and community treatment centers across the assigned region
Represent the client at scientific congresses, investigator meetings, advisory boards, and other scientific forums
Deliver scientific and clinical presentations in response to unsolicited requests
Facilitate interactions between healthcare professionals and internal medical experts
Develop expertise in the hematology treatment landscape, stakeholders, clinical practice patterns, and unmet patient needs
Maintain scientific and clinical expertise in pipeline assets and development programs
Develop and execute regional territory plans aligned with medical strategy
Monitor scientific developments, competitive activities, and emerging data
Translate field insights into actionable recommendations for medical strategy and long-term planning
Partner with Clinical Development teams on early-stage clinical programs and study execution
Support site identification, investigator outreach, and feasibility activities
Collect and communicate field insights for protocol development, clinical strategy, and future study planning
Maintain relationships with study investigators and research sites
Contribute to scientific materials, presentations, and investigator resources
Support investigator-sponsored research and collaborative research opportunities
Collaborate with Medical Affairs, Clinical Development, Commercial, and other cross-functional teams
Assist with advisory boards, scientific meetings, educational activities, medical education, scientific communications, and publication planning
Contribute to competitive intelligence and provide feedback on scientific and clinical developments
Support Medical Affairs systems, processes, documentation standards, and operating procedures
Comply with laws, regulations, industry codes, company policies, training requirements, documentation standards, and regulatory processes

Requirements

What you’ll need

Advanced doctoral degree (MD, PhD, PharmD) or MSc is preferred
5+ years of previous medical affairs experience required, preferably in MSL and/or headquartered based medical affairs role
Postgraduate therapeutic area experience in hematology or oncology is preferred
Knowledge of healthcare systems and understanding of treatment landscape, diagnostic testing and reimbursement in your country/assigned region
Demonstrated expertise in building relationships and participating in credible scientific exchange with multiple audiences
Networking skills and confidence to interact with senior experts on a peer-to-peer level
Experience with clinical trial design, conduct and evaluation
Thorough knowledge of local legal, regulatory, and compliance regulations and guidelines relevant to industry interaction with health care professions
Strong written and verbal communication skills and ability to present medical/scientific information clearly and concisely
Ability to function independently and within a team setting in a dynamic, fast-paced environment
Team-oriented and able to work collaboratively toward common objectives
Biotech experience is a plus
Fluent in English and fluent in the language of a local country is required
Able to travel internationally, up to approximately 70% of the time

Benefits

Comp & perks

Equal employment opportunity policy
Non-discrimination protections based on sex, race, color, religion, national origin, age, disability, marital status, sexual orientation, and veteran status