Medical Science Liaison North East Region

We need to output HTML fragment with sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections if posting has real specific content. We must not repeat job title as heading. No Job ID etc. Remove boilerplate. Must preserve all substantive info. We need to parse posting. Key content: - Intro paragraph: "Join a Team Advancing Innovation in Hematologic Malignancies - Hematology/Oncology Medical Science Liaison IQVIA is seeking experienced Medical Science Liaisons (MSLs) to support a late-stage clinical development program in Acute Myeloid Leukemia (AML). This role provides the opportunity to engage with investigators, hematologists, oncologists, and other healthcare professionals at the forefront of AML research and patient care." - Description of MSL role: "The MSL serves as a field-based scientific resource responsible for facilitating scientific exchange, communicating clinical and translational data, and gathering insights related to disease biology, treatment approaches, measurable residual disease (MRD), relapse risk, and evolving standards of care. The role is intended to strengthen the organization's understanding of the scientific and clinical landscape while supporting Medical Affairs and clinical development objectives through meaningful engagement with the oncology community." - Minimum Requirements: list bullet points. - Preferred Experience: list bullet points. - Position Descriptions and Duties: many bullet points under subheadings: Scientific Exchange & Stakeholder Engagement, Insight Generation & Strategic Medical Intelligence, Clinical Development & Research Support, Medical Affairs Collaboration & Execution. - Then company description: "IQVIA is a leading global provider..." etc. That's boilerplate? Might be considered generic but maybe keep as About the role? Actually it's about company. Could be part of About the role. - Pay: "The potential base pay range for this role is $170,000-$210,000 annually. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits." - No explicit schedule info besides mention of schedule (full or part-time) but not specific schedule. We should not create Schedule section unless posting actually states them. It mentions schedule (full or part-time) as factor but not a defined schedule. Likely we should not create Schedule section. - Benefits: mention "range of health and welfare and/or other benefits". That's vague but still mentions benefits. Could create Benefits section with that statement. - Qualifications: maybe combine Minimum Requirements and Preferred Experience? The instruction: Use headings for Requirements, Qualifications, Skills. We need to decide what goes where. Typically Requirements = minimum requirements. Qualifications = preferred experience? Skills = abilities like communication, CRM, etc. We'll map. - Skills: "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, including healthcare professionals, researchers, and key opinion leaders. Proficiency with business and communication technologies, including CRM platforms, Microsoft Office Suite, Microsoft Teams, and other digital engagement tools. Ability to work independently while collaborating effectively within cross-functional teams." Also maybe "Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines." etc. We must not invent or summarize away detail. Must preserve all substantive info. So we need to include each bullet point as list items. We must not include boilerplate like EEO, fraud warning, etc. Also remove duplicated lines. We need to output only HTML fragment, no /, no markdown fences. Let's structure:

About the role

Join a Team Advancing Innovation in Hematologic Malignancies - Hematology/Oncology Medical Science Liaison. IQVIA is seeking experienced Medical Science Liaisons (MSLs) to support a late-stage clinical development program in Acute Myeloid Leukemia (AML). This role provides the opportunity to engage with investigators, hematologists, oncologists, and other healthcare professionals at the forefront of AML research and patient care. The MSL serves as a field-based scientific resource responsible for facilitating scientific exchange, communicating clinical and translational data, and gathering insights related to disease biology, treatment approaches, measurable residual disease (MRD), relapse risk, and evolving standards of care. The role is intended to strengthen the organization's understanding of the scientific and clinical landscape while supporting Medical Affairs and clinical development objectives through meaningful engagement with the oncology community.

Then maybe a paragraph about IQVIA? Could be part of About the role but might be considered company description. Could include as separate paragraph. But we must not repeat job title as heading. Already not. Now Responsibilities: Could be the Position Descriptions and Duties section. We'll create

Responsibilities

with

• items covering the bullet points under Scientific Exchange & Stakeholder Engagement, Insight Generation & Strategic Medical Intelligence, Clinical Development & Research Support, Medical Affairs Collaboration & Execution. We'll need to capture each bullet. Let's extract bullet points: From Scientific Exchange & Stakeholder Engagement: - 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 approaches, mechanisms of action, clinical trial data, biomarkers, MRD, relapse risk, and evolving standards of care. - Communicate complex clinical and scientific information clearly and credibly to diverse external stakeholders, including physicians, researchers, advanced practice providers, pharmacists, nurses, and multidisciplinary care teams. - Support disease-state education, scientific education programs, advisory boards, investigator meetings, and other medical activities, as appropriate and in accordance with approved materials and compliance requirements. - Tactically execute scientific exchange with healthcare professionals (HCPs), KOLs, formulary committees, and other key stakeholders using client company-approved material. - Identify medical community training and educational needs. Serve as a first and direct point of contact for investigators for the initiation of investigator-initiated studies. - Provide investigators with technical support for study development. - Identify and communicate key clinical and research issues from industry leaders to MSL leadership to help shape company research, development, marketing plans and strategies. - Maintain clinical expertise through aggressive self-education, including attendance at relevant conferences, scientific workshops and review of key journals. - Increase client company visibility with current and future thought leaders. Enhance professional interaction between client company and industry leaders. Insight Generation & Strategic Medical Intelligence: - Capture and communicate actionable field insights related to unmet medical needs, clinical practice patterns, treatment barriers, evidence gaps, stakeholder perceptions, patient identification, sequencing considerations, and adoption considerations. - Synthesize external insights into clear, objective themes and strategic recommendations that inform Medical Affairs, Clinical Development, evidence generation, scientific communications, and launch readiness activities. - Monitor and communicate developments in the competitive landscape, emerging data, clinical trial activity, guideline evolution, congress intelligence, and investigator interests within AML and related hematologic malignancies. - Serve as the voice of external oncology stakeholders internally, ensuring field-derived perspectives are integrated into strategic planning and cross-functional decision-making. Clinical Development & Research Support: - Identify and cultivate relationships with current and potential clinical trial investigators, research centers, cooperative groups, and institutions with expertise in AML, MDS, transplant, cellular therapy, and related hematologic malignancies. - Identify, establish and maintain collaborative relationships with key investigators/ key opinion leaders and institutions strategic to the effective use of company products at a tactical level. - Support scientific discussions related to ongoing and planned clinical development programs, including trial awareness and site engagement activities, as appropriate. - Maintain current knowledge of relevant clinical literature, congress data, trial designs, endpoints, and emerging therapeutic approaches in hematologic oncology. - Identify clinical research opportunities that are consistent with company objectives. Medical Affairs Collaboration & Execution: - Partner with Medical Affairs leadership and cross-functional colleagues to execute the field medical plan - Document scientific interactions and insights accurately and timely in the appropriate CRM or insight management system. - Maintain the highest standards of scientific integrity, ethics, and compliance in all external and internal activities. Now Requirements (minimum): List: - 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 (including being a clinical development scientist in pharma/ biotech) 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, including healthcare professionals, researchers, and key opinion leaders. - Proficiency with business and communication technologies, including CRM platforms, Microsoft Office Suite, Microsoft Teams, and other digital engagement tools. - Ability to work independently while collaborating effectively within cross-functional teams. - Position may require compliance with client-specific site access requirements, including applicable vaccination or health screening protocols. - Familiarity with the planning and execution of clinical trials in oncology and the processes underlying 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. Preferred Experience: - Experience supporting AML, MDS, bone marrow transplant, cellular therapy, cancer immunotherapy, or related hematologic malignancies. - Prior product launch experience within the oncology or rare disease ‘space’. - Existing strong relationships with academic and community hematology/oncology centers. - Networking and partnering with important external customers, including medical thought leaders, academic institutions, NCI Cooperative groups (e.g., ECOG-ACRIN, SWOG, etc.), various clinical trial consortia, large group community practices, medical directors of clinical groups, CMS and insurance carriers, as well as oncology pharmacy directors. Skills: Might overlap with requirements but we can separate: maybe "Strong understanding of healthcare stakeholder segments, treatment landscapes, and market dynamics within oncology." etc. But those already in Requirements. Could still put them under Skills. However we must not duplicate content? The instruction: Preserve ALL substantive information; do NOT invent or summarize away detail. Duplication may be okay if it's in original? But we should avoid repeating same content unnecessarily. Could assign some to Skills that are not already in Requirements: maybe "Proven ability to communicate complex scientific and clinical information effectively to diverse audiences" is already in Requirements. "Proficiency with business and communication technologies" also in Requirements. "Ability to work independently while collaborating effectively within cross-functional teams" also in Requirements. "Strong understanding of healthcare stakeholder segments..." also in Requirements. So Skills may be redundant. Perhaps we can omit Skills section if no unique content. But we need to include a section only when posting has real specific content. If we think Skills are covered, we could still include but risk duplication. Better to omit Skills section. Qualifications: Could be Preferred Experience? Or we could treat Minimum Requirements as Requirements, Preferred Experience as Qualifications. That seems logical. Thus:

  Requirements

  with ul of Minimum Requirements.

  Qualifications

  with ul of Preferred Experience.

  Responsibilities

  with ul of duties.

  About the role

  with intro paragraph and maybe company description.

  Benefits

  with statement about health and welfare benefits.

  Pay

  with pay range statement. We should not include Schedule. Now ensure we don't include boilerplate like "IQVIA is a leading global provider..." maybe we can keep as part of About the role but it's somewhat generic. However it's substantive info about company. Could keep. But we must remove EE