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 that have real content. Must not repeat job title heading. Must not include Job ID etc. Must preserve all substantive info. Remove boilerplate: EEO, fraud warning, etc. Also remove application instructions, navigation, cookie, etc. We need to parse the posting. Key content: - Intro: "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." That's about the role. - Minimum Requirements: list bullet points. - Preferred Experience: bullet list. - Position Descriptions And Duties: sections: Scientific Exchange & Stakeholder Engagement, Insight Generation & Strategic Medical Intelligence, Clinical Development & Research Support, Medical Affairs Collaboration & Execution. Each with bullet points. - Company description: IQVIA is a leading global provider... maybe part of About the role? Could be separate but not required. - 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." - Schedule: Not explicitly given. There's mention of schedule (full or part-time) but not explicit schedule. Might not create Schedule section unless explicit. The instruction: never create Pay/Schedule/Benefits sections unless posting actually states them. Pay is stated. Benefits: mention "range of health and welfare and/or other benefits" - that is a benefit mention. So we can include Benefits section with that statement. Schedule: not explicit; only mention schedule (full or part-time) as factor for pay, but not a defined schedule. Likely we should not create Schedule section. - Requirements: we have Minimum Requirements list. - Qualifications: maybe combine Minimum Requirements and Preferred Experience? The instruction: Use headings for sections like Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide what goes where. Typically Requirements = minimum qualifications. Qualifications = preferred? Skills = abilities like communication, CRM, etc. But we can map. We must not invent or summarize away detail. Must preserve all substantive info. So we need to include all bullet points. We need to avoid duplication. Some bullet points repeat across sections? We'll keep them as they appear. We'll produce sections:

About the role

with paragraph(s) containing the intro and maybe company description.

Responsibilities

with the duties bullet points (maybe grouped under subheadings? But we can just list all duties as

• ...). Could also separate into sub-sections but not required.

  Requirements

  with Minimum Requirements bullet list.

  Qualifications

  with Preferred Experience bullet list.

  Skills

  with abilities: Strong understanding of healthcare stakeholder segments, treatment landscapes, market dynamics within oncology. Proven ability to communicate complex scientific and clinical information effectively to diverse audiences... Proficiency with business and communication technologies... Ability to work independently while collaborating effectively within cross-functional teams. Position may require compliance with client-specific site access requirements... Familiarity with planning and execution of clinical trials... 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. Also maybe "Strong understanding of healthcare stakeholder segments..." etc. Some of these appear in Minimum Requirements as well. But we must preserve all info; duplication is okay? Might be considered duplicate lines; we should avoid duplicated lines. The instruction: remove duplicated lines. So we need to deduplicate identical sentences. Let's see. Minimum Requirements list includes: - 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 list: - 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. Duties bullet points under each subheading. We need to avoid duplication: Some items appear both in Minimum Requirements and maybe also in duties? For example "Strong understanding of healthcare stakeholder segments..." appears only in Minimum Requirements. Not duplicated elsewhere. "Proven ability to communicate complex scientific and clinical information effectively..." appears also maybe in duties? Not exactly. Duties include "Communicate complex clinical and scientific information clearly and credibly to diverse external stakeholders..." similar but not identical. Might be considered duplicate? The instruction: remove duplicated lines. If they are similar but not identical, we keep both? Probably they consider exact duplicate lines. We'll keep both if not exact. We need to ensure we don't include boilerplate: EEO, fraud warning, etc. Also remove "Learn more at https://jobs.iqvia.com" maybe considered navigation? It's a link but not boilerplate; it's part of posting. Might be okay to keep? The instruction: remove cookie/navigation/legal/EEO/equal-opportunity/scam-warning boilerplate, duplicated lines, and application instructions. The link to jobs.iqvia.com is not necessarily boilerplate; it's a reference. Might be considered navigation? Safer to drop it? It's not essential substantive info about the job. Could be considered navigation. I'd drop it. Also drop "IQVIA is proud to be an equal opportunity employer..." etc. Also drop "IQVIA is committed to integrity in our hiring process..." etc. Now we need to output only HTML fragment. Let's craft.

  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. 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.

  Now Responsibilities: combine all duty bullet points. We'll list them as
  • ... each. We need to ensure we capture all duty 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,