Medical Science Liaison – Hemato-Oncology
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Job Description
Medical Science Liaison supporting Amplity’s biopharma clients across European hemato-oncology. Engaging healthcare leaders and advancing AML and MF clinical trials.
Responsibilities:
- Provide fair, balanced, objective scientific information and education to healthcare professionals and internal partners
- Stay informed on current scientific and treatment landscape trends in hemato-oncology
- Build and maintain relationships with healthcare professionals, medical thought leaders, key opinion leaders, investigators, and academic centers
- Identify and engage key stakeholders across multiple European countries
- Drive thought leader engagement and gather competitive intelligence to support strategic decision-making
- Support and drive clinical trial progress in AML and MF, including identifying clinical trial sites and interacting with investigators to enhance patient enrollment
- Act as primary liaison to investigators interested in company-sponsored and investigator-initiated research
- Represent the client at scientific congresses and professional society meetings
- Provide clinical presentations and respond to unsolicited scientific information requests
- Develop and execute territory plans aligned with regional and national plans
- Gather insights from key opinion leaders and report them to support clinical and commercial strategy
- Support local tactical activities, market landscape analysis, competitive intelligence, and identification of therapeutic trends and unmet needs
- Complete assigned tasks, documentation, milestones, and required training
- Help develop and implement MSL clinical education and scientific programs
- Mentor peers and support cross-functional activities
- Document field-based activities and provide special project updates
- Travel approximately 50-60%, including overnight travel as needed
Requirements:
- Advanced degree in clinical specialty (MD, PhD, PharmD) and previous hemato-oncology medical science liaison (MSL) experience strongly preferred
- Candidates with equivalent experience in relevant fields will also be considered
- Previous industry medical affairs experience required, preferably in MSL and/or headquartered based medical affairs role
- Demonstrated experience effectively presenting clinical/scientific information required
- Expert understanding of the health care delivery system and its impact on patient care and regional medical care
- Experience with clinical trial design, conduct and evaluation
- Demonstrated experience supporting clinical trial progress as a field-based member, with a proven ability to engage investigators and drive recruitment
- Experience as an international MSL, with responsibilities across multiple countries desirable
- Ability to relate and work with a wide range of people to achieve results
- Ability to organize and prioritize own work schedule and territory management
- Ability to make decisions which have a significant impact on the department’s credibility, operations, and services
- Ability to create materials such as reports, presentations for inside and outside the organization, and present/speak to groups
- Fluent in English and fluency in the language of a local country is required
- Approximately 50-60% travel is required; overnight travel is required as needed
- Must comply with applicable laws, regulations, guidelines, codes of conduct, company policies, SOPs, and regulatory requirements
Benefits:
- Equal employment opportunities and diversity policy
- Opportunity to work with global healthcare and biopharma companies
- Professional collaboration with clinical, medical affairs, commercial, and consulting teams
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