Summittherapeutics
Medical Science Liaison (France or Belgium)
Summittherapeutics, Baltimore, Maryland, United States,
Job Title: Medical Science Liaison (France or Belgium)
Department: Medical Affairs
Location: Remote France
Summit Therapeutics (Summit) Mission: To build a viable, long-lasting health care organization that assumes full responsibility for designing, developing, trial execution and enrollment, regulatory submission and approval, as well as successful commercialization of patient, physician, caregiver, and societal-friendly medicinal therapy intended to improve quality of life, increase potential duration of life, and resolve serious medical healthcare needs. We accomplish this by building a team of world-class professional scientists and business administrators that apply their experience and knowledge to this mission. We have in-licensed Ivonescimab, a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule. We initiated phase-III clinical studies in Europe and in North America in the following NSCLC indications: Ivonescimab combined with chemotherapy in patients with epidermal growth factor receptor (EGFR)-mutated, locally advanced or metastatic non-squamous NSCLC who have progressed after treatment with a third-generation EGFR tyrosine kinase inhibitor (“HARMONi”) Ivonescimab combined with chemotherapy in first-line metastatic squamous NSCLC patients (“HARMONi-3”) Ivonescimab in first-line PD-L1 High, Metastatic NSCLC (“HARMONi-7”) Overview of Role: The Medical Science Liaison (MSL) is a field-based scientific expert specializing in Immuno-Oncology and related treatment options. They play a strategic role in supporting Summit’s scientific and business objectives throughout the oncology product lifecycle. MSLs act as the primary scientific communicators for Summit within their designated regions, engaging with healthcare professionals and supporting clinical site activities. Combining strong business acumen, clinical expertise, and market awareness, MSLs serve as vital conduits of information to various stakeholders within Summit. Depending on therapeutic needs and product life cycles, their responsibilities may include clinical development and pipeline support. Role and Responsibilities: Develop, execute, and maintain high-impact territory plans, including HCP and Investigator engagement plans, aligned with therapeutic area medical and scientific objectives, focusing on quality. Identify, gain access to, and develop professional, customer-centric relationships with external experts in Immuno-Oncology within the assigned geography. Provide education on disease state, therapeutic landscape, and Summit’s products across the product lifecycle to healthcare providers and researchers. Support clinical development, clinical operations, and research initiatives, including site evaluation and identification, recruitment, investigator meetings, external expert identification, and involving experts to generate scientific data, including investigator-sponsored trials. Participate, monitor, and provide insights to Summit from relevant scientific meetings within the relevant geography. Continuously maintain self-education on market issues and trends, product knowledge, and new therapeutic areas of interest, creating awareness and relationships for Summit in the medical community. Create, maintain, and collaborate on relationships with cross-functional partnerships to develop and execute account plans designed to support and meet shared scientific or business objectives. Actively participate in relevant team meetings, organizational activities, and country-driven medical affairs activities (e.g., advisory boards, Masterclasses, Round-tables). All other duties as assigned. Experience, Education and Specialized Knowledge and Skills: Doctoral degree in health sciences from an accredited university (MD, PhD, PharmD, or equivalent). Significant clinical and/or industry experience in the oncology therapeutic area may be accepted in lieu of education requirements. Lung Cancer clinical experience within the last 5 years is highly desired. A minimum of 5+ years of clinical, scientific/research, or industry-related experience or equivalent is preferred. A minimum of 2+ years experience as a Medical Science Liaison is required. Previous pharmaceutical industry experience within a relevant scientific discipline is preferred. Language requirements:
Proficiency in English and French is required. Additional European language skills are a plus.
The MSL must possess and demonstrate past achievements in:
Understanding, analyzing, and communicating complicated scientific concepts and data. Building credible relationships with prominent HCPs. Independently identifying and translating corporate needs into action plans that achieve objectives. Self-motivation to achieve and exceed goals. Problem-solving and analytic skills. Critical thinking. Ability to work independently.
Other essential requirements:
Meeting healthcare industry representative (HCIR) credentialing requirements to enter facilities and organizations within the assigned territory. Willingness to travel up to 75% of the time. Proficiency in using the standard MS Office suite (e.g., Word, Excel), electronic document management systems, and document review tools. Strong computer and database skills. Attention to detail, accuracy, and confidentiality. Clear and concise oral and written communication skills. Excellent organizational skills. Ability to effectively multi-task or adapt quickly to changing priorities. Ability to manage time-sensitive and highly confidential documents. Ability to prioritize conflicting demands. Ability to work in a fast-paced, demanding, and collaborative environment.
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Department: Medical Affairs
Location: Remote France
Summit Therapeutics (Summit) Mission: To build a viable, long-lasting health care organization that assumes full responsibility for designing, developing, trial execution and enrollment, regulatory submission and approval, as well as successful commercialization of patient, physician, caregiver, and societal-friendly medicinal therapy intended to improve quality of life, increase potential duration of life, and resolve serious medical healthcare needs. We accomplish this by building a team of world-class professional scientists and business administrators that apply their experience and knowledge to this mission. We have in-licensed Ivonescimab, a novel, potential first-in-class investigational bispecific antibody combining the effects of immunotherapy via a blockade of PD-1 with the anti-angiogenesis effects associated with blocking VEGF into a single molecule. We initiated phase-III clinical studies in Europe and in North America in the following NSCLC indications: Ivonescimab combined with chemotherapy in patients with epidermal growth factor receptor (EGFR)-mutated, locally advanced or metastatic non-squamous NSCLC who have progressed after treatment with a third-generation EGFR tyrosine kinase inhibitor (“HARMONi”) Ivonescimab combined with chemotherapy in first-line metastatic squamous NSCLC patients (“HARMONi-3”) Ivonescimab in first-line PD-L1 High, Metastatic NSCLC (“HARMONi-7”) Overview of Role: The Medical Science Liaison (MSL) is a field-based scientific expert specializing in Immuno-Oncology and related treatment options. They play a strategic role in supporting Summit’s scientific and business objectives throughout the oncology product lifecycle. MSLs act as the primary scientific communicators for Summit within their designated regions, engaging with healthcare professionals and supporting clinical site activities. Combining strong business acumen, clinical expertise, and market awareness, MSLs serve as vital conduits of information to various stakeholders within Summit. Depending on therapeutic needs and product life cycles, their responsibilities may include clinical development and pipeline support. Role and Responsibilities: Develop, execute, and maintain high-impact territory plans, including HCP and Investigator engagement plans, aligned with therapeutic area medical and scientific objectives, focusing on quality. Identify, gain access to, and develop professional, customer-centric relationships with external experts in Immuno-Oncology within the assigned geography. Provide education on disease state, therapeutic landscape, and Summit’s products across the product lifecycle to healthcare providers and researchers. Support clinical development, clinical operations, and research initiatives, including site evaluation and identification, recruitment, investigator meetings, external expert identification, and involving experts to generate scientific data, including investigator-sponsored trials. Participate, monitor, and provide insights to Summit from relevant scientific meetings within the relevant geography. Continuously maintain self-education on market issues and trends, product knowledge, and new therapeutic areas of interest, creating awareness and relationships for Summit in the medical community. Create, maintain, and collaborate on relationships with cross-functional partnerships to develop and execute account plans designed to support and meet shared scientific or business objectives. Actively participate in relevant team meetings, organizational activities, and country-driven medical affairs activities (e.g., advisory boards, Masterclasses, Round-tables). All other duties as assigned. Experience, Education and Specialized Knowledge and Skills: Doctoral degree in health sciences from an accredited university (MD, PhD, PharmD, or equivalent). Significant clinical and/or industry experience in the oncology therapeutic area may be accepted in lieu of education requirements. Lung Cancer clinical experience within the last 5 years is highly desired. A minimum of 5+ years of clinical, scientific/research, or industry-related experience or equivalent is preferred. A minimum of 2+ years experience as a Medical Science Liaison is required. Previous pharmaceutical industry experience within a relevant scientific discipline is preferred. Language requirements:
Proficiency in English and French is required. Additional European language skills are a plus.
The MSL must possess and demonstrate past achievements in:
Understanding, analyzing, and communicating complicated scientific concepts and data. Building credible relationships with prominent HCPs. Independently identifying and translating corporate needs into action plans that achieve objectives. Self-motivation to achieve and exceed goals. Problem-solving and analytic skills. Critical thinking. Ability to work independently.
Other essential requirements:
Meeting healthcare industry representative (HCIR) credentialing requirements to enter facilities and organizations within the assigned territory. Willingness to travel up to 75% of the time. Proficiency in using the standard MS Office suite (e.g., Word, Excel), electronic document management systems, and document review tools. Strong computer and database skills. Attention to detail, accuracy, and confidentiality. Clear and concise oral and written communication skills. Excellent organizational skills. Ability to effectively multi-task or adapt quickly to changing priorities. Ability to manage time-sensitive and highly confidential documents. Ability to prioritize conflicting demands. Ability to work in a fast-paced, demanding, and collaborative environment.
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