INSIGHTEC Ltd.
Jr Medical Science Liaison - MRgFUS in Neurosciences Europe - Remote
INSIGHTEC Ltd., Baltimore, Maryland, United States,
Jr Medical Science Liaison - MRgFUS in Neurosciences
What you will be doing:Independently establish and maintain robust relationships across neuroscience-related specialties, key medical groups, associations, and patient advocacy organizations.Organize and support a cohesive and effective scientific communication and community-building strategy executed through multi-modal clinical education channels, including investigator meetings, publications, presentations, congresses, advisory boards, CME, speaker bureaus, and other channels.Maintain up-to-date knowledge as a therapeutic and disease expert within the dynamic scientific and clinical environment of interest to the company.Engage in high-level scientific discussions with external partners to maintain a reliable presence with scientific leaders and partner institutions to ensure regular medical and scientific contact with the Company (70% of the time).Serve as an educational resource for healthcare providers by delivering relevant scientific data through clear and personalized engagement.Gather feedback, data, or information during routine activities that can help the Company better comprehend the medical or scientific needs, priorities, or concerns of healthcare practitioners (HCPs) and/or patients.For Company-Sponsored Trials, collaborate and assist Clinical and Regulatory Affairs in reviewing study sites, identify potential investigators to participate in clinical development programs, identify barriers to patient enrollment and retention efforts to achieve study milestones, address questions from investigators and provide information regarding participation in company-sponsored clinical studies.For Investigator-Initiated Trials, support external academic partners in the development of site-initiated clinical research proposals:Assist external partners in the submission of research proposals.Assist Company in the assessment of partner institutions (environment, resources, ability to conduct the proposed trial, and ability to publish clinically meaningful data of interest to the Company).Communicate internally to Company leadership the purpose, advantages, limitations, duration, and potential deliverables of the planned trial.Assist in identifying grants and other sources of funding to support external collaborators.Engage in scientific congresses and other medical meetings, with careful pre-meeting preparation to ensure maximum representation of available scientific data, facilitate scientific and data exchange, and collect meaningful insights.Working according to Insightec Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.What you have:MD, PhD or equivalent with specialization in movement disorders, neurosciences or a relevant field is preferred.2+ years of experience within Medical Device and/or Biopharma Industry is a plus.Demonstrated ability and comfort-level interacting with scientific leaders, including physicians, scientists, and other leaders at academic institutions.Proven ability to review, interpret and present scientific information and demonstrated critical thinking skills.Experience in investigator-initiated clinical trials, clinical manuscript and/or grant writing is preferred.Must be self-directed and comfortable with identifying and presenting strategies to leadership for new initiatives and activities.Willingness and ability to travel with at least 50% travel required.
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What you will be doing:Independently establish and maintain robust relationships across neuroscience-related specialties, key medical groups, associations, and patient advocacy organizations.Organize and support a cohesive and effective scientific communication and community-building strategy executed through multi-modal clinical education channels, including investigator meetings, publications, presentations, congresses, advisory boards, CME, speaker bureaus, and other channels.Maintain up-to-date knowledge as a therapeutic and disease expert within the dynamic scientific and clinical environment of interest to the company.Engage in high-level scientific discussions with external partners to maintain a reliable presence with scientific leaders and partner institutions to ensure regular medical and scientific contact with the Company (70% of the time).Serve as an educational resource for healthcare providers by delivering relevant scientific data through clear and personalized engagement.Gather feedback, data, or information during routine activities that can help the Company better comprehend the medical or scientific needs, priorities, or concerns of healthcare practitioners (HCPs) and/or patients.For Company-Sponsored Trials, collaborate and assist Clinical and Regulatory Affairs in reviewing study sites, identify potential investigators to participate in clinical development programs, identify barriers to patient enrollment and retention efforts to achieve study milestones, address questions from investigators and provide information regarding participation in company-sponsored clinical studies.For Investigator-Initiated Trials, support external academic partners in the development of site-initiated clinical research proposals:Assist external partners in the submission of research proposals.Assist Company in the assessment of partner institutions (environment, resources, ability to conduct the proposed trial, and ability to publish clinically meaningful data of interest to the Company).Communicate internally to Company leadership the purpose, advantages, limitations, duration, and potential deliverables of the planned trial.Assist in identifying grants and other sources of funding to support external collaborators.Engage in scientific congresses and other medical meetings, with careful pre-meeting preparation to ensure maximum representation of available scientific data, facilitate scientific and data exchange, and collect meaningful insights.Working according to Insightec Quality Policy, relevant Quality Procedures & Standards, and privacy & safety rules.What you have:MD, PhD or equivalent with specialization in movement disorders, neurosciences or a relevant field is preferred.2+ years of experience within Medical Device and/or Biopharma Industry is a plus.Demonstrated ability and comfort-level interacting with scientific leaders, including physicians, scientists, and other leaders at academic institutions.Proven ability to review, interpret and present scientific information and demonstrated critical thinking skills.Experience in investigator-initiated clinical trials, clinical manuscript and/or grant writing is preferred.Must be self-directed and comfortable with identifying and presenting strategies to leadership for new initiatives and activities.Willingness and ability to travel with at least 50% travel required.
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