Medical Science Liaison jobs in Israel

Job Description Summary #LI-Hybrid This role is based in Israel. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. The Medical Scientific Liaison (MSL) acts as a scientific ambassador, enabling high-quality, peer-to-peer scientific exchange with Healthcare Professionals (HCPs) and Medical Experts (MEs), within the field of Immunology. The role exists to strengthen Novartis’ scientific presence, support evidence-based decision making, and inform medical strategy through high-quality insight generation. MSLs provide deep therapeutic area and product understanding, translate emerging science into meaningful dialogue, and support internal teams with clinical data interpretation. MSL is field-based role and needs to operate primarily in the field, the MSL bridges scientific needs from clinical practice with internal strategy to improve patient outcomes and reinforce Novartis’ reputation for scientific excellence. Job Description Key responsibilities • Execute Medical Expert engagement plans aligned with Therapeutic Area strategic priorities and ensure appropriate identification, mapping, and involvement of MEs and key accounts where medical needs, scientific questions, or evidence gaps are identified. • Conduct unbiased, evidence-based, peer-to-peer scientific exchange with HCPs and MEs, sharing and contextualizing up-to-date medical information, disease area knowledge, clinical data, and publications. • Support ME/HCP education activities, including hospital staff meetings, regional scientific events, symposia, and internal or external educational initiatives. • Systematically collect, synthesize, and communicate actionable external insights from clinical practice, scientific discussions, and competitive activities to inform local and regional medical strategy. • Contribute scientific insights to country medical plans and disease area strategies while maintaining strong understanding of the therapeutic landscape, emerging data, and competitor environment. • Support evidence generation and clinical research by identifying and qualifying potential study sites and facilitating communication between sites and internal teams to optimize study execution. • Build and maintain strong partnerships with Medical Experts, scientific societies, academic institutions, and other stakeholders to strengthen scientific leadership and collaboration in the Therapeutic Area. • Act as a credible scientific resource for internal partners by providing clinical context, data interpretation, training, and cross-functional scientific support. • Shape joint value creation initiatives, evidence-based collaborations, and multistakeholder partnerships that strengthen the medical ecosystem and Novartis’ scientific reputation. • Ensure all engagements, materials, activities, CRM documentation, reporting, and activity tracking meet ERC, regulatory, medical governance, and company guidance requirements. Requirements • Advanced scientific degree (MD, PharmD, DVM, DMD, PhD in Life Sciences) or equivalent is mandatory; • Proficient Hebrew and English, both written and spoken • Strong communication & interpersonal skills • Strong planning, prioritization, and territory management capabilities, with proven ability to navigate complexity • Agile, resilience, a growth mindset • Ability to partner effectively in a matrix environment, influence without authority, and build credible, collaborative relationships across internal and external stakeholders. • Strong scientific and clinical data interpretation capabilities, with the ability to effectively present and communicate complex scientific evidence and emerging medical insights across diverse audiences. • Ability to build credible, trusted relationships with healthcare professionals About Novartis Israel: Novartis is a leading pharmaceutical company renowned for its innovation. In Israel, we pioneered the introduction of advanced cell and gene therapies. Our commitment to research and development spans a wide range of therapeutic areas, including oncology, chronic conditions, and rare diseases. We take pride in being a proactive partner, contributing to the advancement of healthcare solutions. As a global pharmaceutical leader headquartered in Switzerland, Novartis is among the largest pharmaceutical companies in Israel. Our mission is to lead in delivering innovative medicines to patients across the country. We are dedicated to fostering a dynamic work environment that promotes personal development and professional growth. Commitment To Diversity & Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Skills Desired Biostatistics, Clinical Research, Clinical Study Reports, Curious Mindset, Customer Relationship Management (CRM) Software, Disease Management, Drug Development, Epidemiology, IT Tools, Medical Information, Medical Research, Medical Writing, Product Placement

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. We seek an Executive Director/Vice President for our Medical Science and Strategy Team - Metabolic. The role can be based in the EMEA region but will require travel to China (or relocation could be considered). The position requires proven abilities to drive both strategic and measurable business outcomes. The incumbent’s Metabolic track record expertise is required to be extensive and ensure recognition as peer of their Pharmaceutical Industry equivalents. This position is playing a key part in the future success of the PPD clinical research business of Thermo Fisher Scientific, as it seeks to continue its track record of successful growth and expand Industry leading position in Metabolic. Medical Science & Strategy physicians are subject matter experts who support sales for proposals and bid defences, engaging clients senior medical / scientific leadership in discussions and training internal staff on medical and therapeutic requirements of the proposals. The role comprises four major functions: • First, the incumbent is responsible for ensuring the highest possible quality of input into significant requests for proposals (RFPs), including: • Development strategy and regulatory issues • Drug class issues • Protocol and indication considerations, including safety • Team education on indication • Interactions with client’s physicians and / or client area indication leaders prior to and during bid defences • Identifying business opportunities for the PPD clinical research business • Secondly, the incumbent is responsible for supporting outstanding input into other areas of the PPD clinical research business activities, including: • Pro-active client engagement: peer-to-peer interactions with therapeutic area leaders and senior directors of companies whose portfolio contains drugs of business interest • Strategic alliance development & support • Client governance and advisory boards • Through PPD’s consulting practice, the incumbent will provide Industry gold standard product development plans, and top-level design of clinical trial protocols that are required in the development plan. • Thirdly, the incumbent will be responsible for providing therapeutic and developmental expertise to internal teams, including: • Indication specific training for clinical teams • Guidance during clinical trials executions • Investigator Brochure, clinical study report, NDA / MAA clinical packages development, and other regulatory briefing documents authoring and review • Contribute to design and reporting of feasibility studies • Liaise with investigators and KOLs • Mentor and supervise clinical scientists • Finally, the incumbent will participate in multidisciplinary teams and working groups to contribute to innovative initiatives based on their specific knowledge, expertise and interest. Minimum Qualifications: • MD or equivalent required • Certified in a medical specialty or subspecialty related to metabolic disorders (i.e. Endocrinology, Cardiology, Internal Medicine) with at least 5+ years’ experience in pharmaceutical industry leading clinical development of at least one asset from discovery through registration. • Proficient in spoken and written English and Mandarin • Active medical license preferred but not required. Knowledge, Skills and Abilities: • Able to work in a matrix organization. • Able to demonstrate the following key high-level high-performance behaviors: decisive, customer driven, flexible thinking, smart-risk taking and continuous improvement. • Leads, influences and motivates staff within and across departments. • Strong in presenting and communicating complex information clearly. • Able to deal with sensitive and confidential issues. • Possesses a “can do” attitude and is capable of implementing and following through on activities / projects. • Flexibility to travel domestically and internationally What we offer: • Full time position • Competitive salary and benefits • Work diversity, exposure to several assets in different stages of clinical development from several clients • Mentorship and training • Exciting work environment About the PPD clinical research business of Thermo Fisher Scientific: Our mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today!

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future. We seek an Executive Director/Vice President for our Medical Science and Strategy Team - Oncology. The role can be based in the EMEA region but will require travel to China (or relocation could be considered). The position requires proven abilities to drive both strategic and measurable business outcomes. The incumbent’s Oncology track record expertise is required to be extensive and ensure recognition as peer of their Pharmaceutical Industry equivalents. This position is playing a key part in the future success of the PPD clinical research business of Thermo Fisher Scientific, as it seeks to continue its track record of successful growth and expand Industry leading position in Oncology. Medical Science & Strategy physicians are subject matter experts who support sales for proposals and bid defences, engaging clients senior medical / scientific leadership in discussions and training internal staff on medical and therapeutic requirements of the proposals. The role comprises four major functions: • First, the incumbent is responsible for ensuring the highest possible quality of input into significant requests for proposals (RFPs), including: • Development strategy and regulatory issues • Drug class issues • Protocol and indication considerations, including safety • Team education on indication • Interactions with client’s physicians and / or client area indication leaders prior to and during bid defences • Identifying business opportunities for the PPD clinical research business • Secondly, the incumbent is responsible for supporting outstanding input into other areas of the PPD clinical research business activities, including: • Pro-active client engagement: peer-to-peer interactions with therapeutic area leaders and senior directors of companies whose portfolio contains drugs of business interest • Strategic alliance development & support • Client governance and advisory boards • Through PPD’s consulting practice, the incumbent will provide Industry gold standard product development plans, and top-level design of clinical trial protocols that are required in the development plan. • Thirdly, the incumbent will be responsible for providing therapeutic and developmental expertise to internal teams, including: • Indication specific training for clinical teams • Guidance during clinical trials executions • Investigator Brochure, clinical study report, NDA / MAA clinical packages development, and other regulatory briefing documents authoring and review • Contribute to design and reporting of feasibility studies • Liaise with investigators and KOLs • Mentor and supervise clinical scientists • Finally, the incumbent will participate in multidisciplinary teams and working groups to contribute to innovative initiatives based on their specific knowledge, expertise and interest. Minimum Qualifications: • MD or equivalent required • Certified Oncologist with at least 5+ years’ experience in pharmaceutical industry leading clinical development of at least one asset from discovery through registration. • Proficient in spoken and written English and Mandarin • Active medical license preferred but not required. Knowledge, Skills and Abilities: • Able to work in a matrix organization. • Able to demonstrate the following key high-level high-performance behaviors: decisive, customer driven, flexible thinking, smart-risk taking and continuous improvement. • Leads, influences and motivates staff within and across departments. • Strong in presenting and communicating complex information clearly. • Able to deal with sensitive and confidential issues. • Possesses a “can do” attitude and is capable of implementing and following through on activities / projects. • Flexibility to travel domestically and internationally What we offer: • Full time position • Competitive salary and benefits • Work diversity, exposure to several assets in different stages of clinical development from several clients • Mentorship and training • Exciting work environment About the PPD clinical research business of Thermo Fisher Scientific: Our mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today!

MSL Introduction to role: Are you ready to turn scientific dialogue into real-world patient impact across your territory? Do you want to use your scientific credibility and business acumen to shape treatment pathways and inform brand strategy while staying close to the evidence? As an MSL at AstraZeneca, you will build trusted scientific partnerships with Key External Experts and healthcare professionals, translating the latest data into meaningful insights and actions. You will be 60% field-based, engaging face-to-face across your territory and partnering closely with an office-based Medical Affairs Manager for your therapeutic area to connect scientific strategy with on-the-ground reality. In this role, you will help align medical and commercial objectives without compromising on ethics—fueling our growth and enabling continued investment in research. Your work will ensure that the right data reaches the right stakeholders at the right time, improving decision-making and, ultimately, patient outcomes. Accountabilities: Scientific Exchange and Insight Generation: Conduct high-quality scientific discussions with KEEs and HCPs; gather and synthesize field insights to inform medical strategy and brand planning. Therapeutic Area Mastery: Maintain up-to-date expertise on the TA, treatment paradigms, and competitor data through literature review, congress attendance, and expert engagement. Account Plan Execution: Deliver medical components of account plans to time and budget, ensuring activities address identified gaps and opportunities. Expert Partnership Development: Build deep, trust-based relationships with KEEs; map interests, identify collaboration opportunities, and support local practice change. Evidence Discussion and Data Gap Identification: Present and discuss key data sets to uncover evidence gaps, patient pathways, and unmet needs aligned to TA strategy. Scientific Events and Education: Initiate and co-create scientific events with KEEs; lead journal clubs and one-to-one scientific exchanges that elevate disease and therapy understanding. Digital Medical Engagement: Produce compliant scientific digital content (e.g., newsletters, approved emails) as part of integrated medical plans to broaden reach and impact. Field Intelligence and Internal Collaboration: Share actionable insights with cross-functional teams; contribute to the core strategic plan and educate key account managers and colleagues on disease and therapies. Clinical Study and Early Access Support: Support AZ-sponsored clinical studies (site selection and initiation) and contribute to bridging/early access programs where relevant. Externally Sponsored Research and Funding Stewardship: Manage ESRs, grants, donations, and third-party scientific sponsorships with rigor and transparency. Real-World Evidence and Care Transformation: Identify partners, including KEEs and Sick Funds, to develop real-world data initiatives and care-improvement projects that enable local practice change. Network and Best Practice Sharing: Collaborate with MSLs across countries and TAs to exchange best practices and continuously evolve the role. Congress Participation: Attend national congresses and, as required, represent the TA at international meetings to bring back insights and strengthen external networks. Medical Information and Documentation: Respond to medical information requests via approved platforms; document all interactions thoroughly and on time in the designated systems. Compliance and Continuous Improvement: Complete all training; uphold AZ policies and external codes; seek feedback through training and joint field visits to refine communication and insight-gathering skills. Essential Skills/Experience: - MD/PharmD/PhD/DVM or equivalent - Significant and robust experience with searching, handling, assimilating, synthesizing, reporting, and presenting scientific data in the healthcare sector - Quick self-learner, ability, and willingness to work in a team and independently. - National mobility and flexibility in attendance of local events outside of working hours - Ability to multitask effectively, demonstrate strong time management skills, and excel under pre-specified deadlines - Excellent relational and communication skills - Ability to build and maintain strategic partnerships with a diverse range of stakeholders. - Takes initiative and proactive were needed while conscious of compliance and process rules in the company - Presentation skills - Medical integrity and ethical balance - Fluent knowledge of English (verbal and written) Desirable Skills/Experience: - Experience in and knowledge of pharmaceutical medical and marketing processes - Knowledge of therapeutic area. Broad employability in other TAs is an asset. - Experience in moderation of meetings with HCPs - Business Acumen - Proven Project management skills - Digital capabilities, experience in creating digital assets - Ability to rapidly shift between multiple projects and managing field-office workload - Experience in production of scientific events - Ability to distinguish between the main and the minor Why AstraZeneca: Here, science and strategy meet to accelerate impact for patients. You will join a team that brings medical experts, commercial thinkers, and innovators into the same room to unlock bold ideas—always guided by evidence and strong ethics. We move with agility, learn fast from what works and what doesn’t, and stay close to a broad, science-led pipeline that keeps our work varied and meaningful. Your insights from the field will shape decisions across the business, helping us invest wisely in research while improving how patients are diagnosed, treated, and cared for. We value kindness alongside ambition and collaboration over ego, so you can stretch your capabilities with the support of world-class colleagues connected across our global network. Call to Action: Step into a role where your scientific voice drives better care—show us how you will elevate partnerships, sharpen strategy, and deliver impact for patients today! Date Posted 30-Jul-2026 Closing Date 31-Oct-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Job Description Summary As a Medical Science Liaison (MSL), you will serve as a trusted scientific partner to leading Cardiology Key Opinion Leaders (KOLs) and healthcare professionals, driving meaningful scientific exchange and advancing evidence-based patient care. In this highly visible field-based role, you will communicate complex clinical and scientific information with accuracy and credibility, helping to deepen understanding of products, therapeutic areas, and emerging data. You will collaborate closely with healthcare providers to address scientific inquiries, deliver educational insights, and support informed clinical decision-making. Internally, you will work cross-functionally with Medical Affairs, Clinical, Commercial, and other teams, providing medical expertise and strategic input across a variety of initiatives. This role will support the Central territory. Our Pharmaceutical Diagnostics (PDx) business is the number one global supplier of contrast media and molecular imaging agents used to enhance medical imaging exams. Used throughout all major disease area diagnostic and treatment pathways, PDx products support three patients every second around the world. Job Description Essential Responsibilities • Per the Cardiology Medical engagement plan, interact with KOLs to communicate and advance GE’s Cardiology medical plans and initiatives. • Communicate clinical/scientific insights as well as research concepts from KOLs back to medical affairs team members within the organization, for further evaluation. Communication is consistent with bidirectional scientific exchange; encompassing data dissemination and education, as well as the gleaning and capturing of HCP insights. • Participate at regional and national cardiology conferences; actively contribute to conference planning, scientific session coverage and development of scientific summary subsequent to conferences. • • With oversight from Cardiology Medical Director/ Care Area Lead, provide support to unsolicited investigator sponsored research proposals as well as Company sponsored research. • Participate in identification and training of participants in the Company’s speaker’s bureau members, when applicable. • Demonstrate full awareness of and compliance with all SOPs and applicable laws and regulations as they apply to this job type/position. Proactively identify and report any quality or compliance concerns and take immediate action as required. • Participate in preparation and delivery of training materials to support new and existing medical staff on diagnostic imaging agents used in Cardiology and emerging clinical evidence. • Provide medical expertise and support to projects led by US/Canada Medical Affairs and other cross-functional projects, such as advisory boards, educational activities, clinical study support as necessary. Required Qualifications: • Advanced degree is (MS, PhD, PharmD, MD) • 2+ years Pharmaceutical/Healthcare industry experience (preferably as an MSL with some experience in Cardiology, Radiology, Nuclear Medicine. • A proactive leader who translates strategy into timely, impactful outcomes. • Experience delivering professional presentations through listed lectures or evidence of teaching • Requires ability to travel in excess of 70% (Including some weekends) • Required location within territory: (ND,SD,NE,KS,IA,MO,KY,TN) local to major airport. Desired Characteristics: • Ideal location: ( Kansas City, Louisville,Nashville) • Results-oriented team player who thrives in collaborative environments while maintaining a high level of accuracy and attention to detail. • Five or more years’ experience in a medical affairs/MSL role. • Nuclear cardiology experience preferred. • Location near major metro area with easy airport access. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership –always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support. #LI-MA4 We will not sponsor individuals for employment visas, now or in the future, for this job opening.

 Additional Information GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees. Relocation Assistance Provided: No