Medical Science Liaison

• Engage national oncology healthcare access decision makers through credible, non-promotional, outcomes-focused scientific exchange
• Identify key national oncology healthcare decision makers and serve as the primary medical liaison between AbbVie and healthcare decision makers
• Build relationships to understand customer needs and facilitate generation of real-world evidence consistent with medical planning
• Advance field scientific strategies and serve as a role model to field medical peers
• Serve as medical lead within key account management teams for assigned accounts
• Lead oncology therapeutic-area and healthcare-landscape strategic planning and issue resolution
• Provide customized communication of scientific, health outcomes, and health policy information
• Document and communicate observations that contribute to Scientific Intelligence
• Identify emerging scientific, health economic, and health policy trends and incorporate learnings into strategy and objectives
• Serve as primary interface and initial contact for large-scale real-world evidence opportunities with national healthcare decision makers
• Anticipate and address population-level scientific, outcomes research, and health policy needs
• Facilitate scientific exchange between AbbVie medical leadership, Medical Affairs and Health Impact, therapeutic-area medical directors, HEOR, and senior priority-account leaders
• Maintain and enhance clinical, scientific, and healthcare-landscape expertise
• Participate in therapeutic advisory activities involving marketed and investigational products across the product lifecycle
• Train, coach, and mentor MOSLs
• Provide guidance and strategic direction to MOSLs supporting key access organizations
• Collaborate with cross-functional partners and the In-Field Team to support aligned national execution
• Link scientific engagement to measurable shifts in decision-making and quality of product access

National Medical Outcomes Science Liaison

• Develop, enhance, and leverage key opinion leader relationships in therapeutic areas of interest to the company
• Enhance scientific expertise of external stakeholders via scientific exchange
• Provide key field insights and competitive intelligence to Medical Affairs and cross-functional teams
• Attend national and regional medical conferences and report findings to internal stakeholders
• Provide medical coverage at company events and booths
• Respond to medical information requests from healthcare professionals
• Assist in developing and delivering training on scientific topics
• Assist in developing and executing advisory board meetings and focus groups
• Provide payer presentations in key accounts
• Collaborate with R&D and Clinical teams on research projects
• Liaise between investigators and internal stakeholders for investigator-initiated research
• Participate in Medical Affairs and cross-functional projects
• Establish strong account and healthcare professional relationships
• Ensure accurate travel and expense reporting
• Ensure adherence to TerSera policies and Code of Conduct
• Maintain a safe, positive, and professional working environment

• 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 to 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
• Execute scientific exchange with healthcare professionals, KOLs, formulary committees, and other key stakeholders using approved materials
• Identify medical community training and educational needs
• Serve as a first point of contact for investigators initiating investigator-initiated studies
• Provide investigators with technical support for study development
• Communicate clinical and research issues to MSL leadership to help shape research, development, marketing plans, and strategies
• Maintain clinical expertise through self-education, conferences, scientific workshops, and journal review
• Capture and communicate actionable field insights regarding unmet needs, clinical practice, treatment barriers, evidence gaps, stakeholder perceptions, patient identification, sequencing, and adoption
• Synthesize external insights into strategic recommendations for Medical Affairs, Clinical Development, evidence generation, scientific communications, and launch readiness
• Monitor competitive developments, emerging data, clinical trial activity, guideline evolution, congress intelligence, and investigator interests
• Identify and cultivate relationships with clinical trial investigators, research centers, cooperative groups, and institutions
• Support scientific discussions related to clinical development programs, trial awareness, and site engagement
• Identify clinical research opportunities consistent with company objectives
• Partner with Medical Affairs leadership and cross-functional colleagues to execute the field medical plan
• Document scientific interactions and insights accurately and timely in CRM or insight management systems
• Maintain scientific integrity, ethics, and compliance

Medical Science Liaison, Midwest – Central Region

• Build and maintain relationships with key opinion leaders in optometry and ophthalmology within the assigned territory
• Serve as the primary Medical Affairs point of contact for scientific exchange and educational engagement through virtual and in-person interactions
• Gather actionable field insights and communicate findings to internal stakeholders to help shape medical strategy and initiatives
• Deliver disease state and scientific education to healthcare providers and practice staff
• Support educational initiatives within optometry schools and ophthalmology residency programs
• Provide guidance regarding investigator-initiated research processes and medical information resources
• Identify and recommend expert faculty and advisors for educational programs, advisory boards, publications, clinical research, and other Medical Affairs initiatives
• Develop and execute KOL engagement plans and attend local, regional, and national scientific meetings
• Collaborate with professional societies and relevant healthcare organizations within the territory
• Present scientific and clinical information to healthcare stakeholders, including payer audiences
• Contribute leadership and expertise to Medical Affairs projects and cross-functional initiatives
• Support continuous improvement efforts related to training, insights generation, and field medical operations
• Lead and facilitate scientific discussions and educational programs focused on disease awareness and patient care
• Collaborate with Clinical Development, Commercial, Medical Information, and Training
• Provide support for clinical development activities and study-related initiatives when needed
• Maintain territory plans, KOL profiles, CRM documentation, and budget accountability

Medical Science Liaison, Ophthalmology

• Present scientific and clinical information on Alcon products
• Gather external insights to influence company strategies
• Develop and maintain peer-to-peer relationships with medical experts and key opinion leaders
• Support development and adoption of Alcon products through evidence-based scientific exchange
• Provide general medical information to practitioners and Alcon associates
• Respond to unsolicited requests for medical information
• Engage in scientific discussions about Alcon product data
• Implement medical projects and navigate investigator trials from inception to publication
• Maintain thorough knowledge of Alcon products and current medical/scientific research
• Work with Med Info and Med Safety to resolve escalated product complaints and medical safety issues
• Participate in adverse event reporting and safety responsibility monitoring
• Direct phase III and IV human clinical trials, monitor protocol adherence, and determine study completion
• Provide reporting information for regulatory agency submissions
• Serve as medical consultant to marketing, commercial, research, and regulatory teams
• Act as consultant/liaison with corporations under licensing agreements
• Sign off on product safety reviews
• Interface with Medical Affairs and departments including Commercial, Quality Assurance, Research and Development, Regulatory Affairs, and Market Access
• Follow GxP regulations, SOPs, documentation, quality control, and required training requirements

Medical Science Liaison jobs in Illinois

National Medical Outcomes Science Liaison