Medical Science Liaison jobs in Israel

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!

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