GlaxoSmithKline
Medical Science Liaison (Oncology) (KS, IA, NE, MO Territory)
GlaxoSmithKline, Topeka, Kansas, United States,
Site Name:
USA - Kansas - Kansas City West, USA - Iowa - Des Moines, USA - Missouri - Kansas City, USA - Nebraska - Omaha Posted Date:
Nov 14 2024 As an Oncology Medical Science Liaison, you will be the scientific expert for a group of medicines in the Hematology therapeutic area within the assigned territory to conduct balanced, peer-to-peer, scientific dialogue with external experts. The territory encompasses: ( Kansas, Iowa, Nebraska, Missouri) This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Interface and provide value across a continuum of both Internal and External Stakeholders (External Experts and other healthcare professionals within assigned geography/therapy area, investigators and potential investigators, and formulary decision makers) in a non-promotional manner and be responsive to unsolicited inquiries. Respond orally or by providing appropriate written materials to unsolicited requests for on- or off-label information or safety concerns that may have been asked of GSK sales staff or Medical and adhering to all policies and procedures regarding the provision of medical information. Gain valuable insight and feedback from the healthcare community on GSK products and services, medical and scientific information which can help guide research, development and service provision to benefit GSK’s customers and patients. Contribute in a manner that is always consistent with GSK Values and expectations demonstrating Courage, Accountability, Development, and Teamwork. Work with medical colleagues and other business partners to identify External Experts, professional groups, decision makers and other key stakeholders in the assigned therapy area and or geography. Attend and contribute (if required) to medical portion of regional account planning/training sessions. Maintain expertise in the evolving scientific / therapeutic area and in competitor medicines. Respond compliantly to unsolicited information requests from healthcare professionals and associated individuals regarding licensed or un-licensed GSK medicines and indications; ensure all medical information responses are factual, fair and balanced, scientifically rigorous and strictly comply with GSK standards and policies and with local codes of practice, guidelines and laws to ensure the strictest requirements are met. Disseminate important safety information to the healthcare profession as directed by the Medical Affairs or Research and Development teams or the Dear Healthcare Provider Letter (DHPL) process. Scientific exchange for a GSK medicine that is on label or consistent with the label to inform and educate HCPs on the appropriate use of our medicines in patients. Deliver scientific / pipeline presentations to formulary committees and HCPs per documented unsolicited request. Support clinical development activities and programs including GSK and Investigator sponsored studies as well as collaborating with R&D staff to improve site performance. Provide general insight into GSK research interests and field inquiries regarding investigator sponsored scientific or clinical research projects. Attend both national and regional scientific/medical meetings to gain medical voice of the customer on recent data being presented on products and disease states of interest to GSK. Conduct individual discussions and meetings with steering committee members, advisory board members, consultants etc., on topics related to the work being conducted with GSK (e.g. for clinical research investigators, the conduct or publication of clinical research sponsored by GSK). Provide scientific training for GSK sales representatives regarding GSK products and the conditions they treat utilizing approved Sales Training materials. Provide training to individual HCPs to prepare them to speak on behalf of GSK and assist with GSK-sponsored speaker training events. Partner with matrix colleagues (e.g. sales, marketing, market access, etc.) to ensure strategies and business plans are both patient and business focused and adding value to the external expert. Basic Qualifications: Pharm D, PhD, or M.D. A minimum of 2 years clinical practice and/or pharmaceutical industry experience. A minimum of two years’ experience applying knowledge of pharmacology and pharmacotherapy in humans in a clinical setting. Must live in designated territory and near a major airport. Must be willing to travel up to 70%. Preferred Qualifications: Hematology Oncology experience. Multiple Myeloma or Myleofibrosis experience. Nurse Practitioner or Physician Assistant with oncology background may be considered. Previous clinical experience in situations where direct/or indirect decision-making authority for patient care was demonstrated. At least one year of experience in pharmacology and pharmacotherapy in humans and applying this knowledge in a clinical setting. Above average computer literacy, including experience with software applications. Excellent interpersonal skills in both one on one and group settings. Proven ability to work autonomously and independently with time management skills to effectively manage field-based responsibilities. Strong communication skills: demonstrated ability to identify opportunities for medical engagement and develop a set of scientific engagement goals. Strong presentation skills. Preferred location with easy access to an airport that serves the states within assigned territory. Clear understanding of clinical research methodologies and a demonstrated ability to translate scientific, clinical and safety research studies in an effective credible manner. Ability to maintain a command of a large amount of scientific information across multiple products and show effective written/verbal communication skills. Ability to develop and maintain strong trusted relationships, with key decision makers. Demonstrated customer-focus, problem solving abilities and strong conflict resolution skills.
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USA - Kansas - Kansas City West, USA - Iowa - Des Moines, USA - Missouri - Kansas City, USA - Nebraska - Omaha Posted Date:
Nov 14 2024 As an Oncology Medical Science Liaison, you will be the scientific expert for a group of medicines in the Hematology therapeutic area within the assigned territory to conduct balanced, peer-to-peer, scientific dialogue with external experts. The territory encompasses: ( Kansas, Iowa, Nebraska, Missouri) This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Interface and provide value across a continuum of both Internal and External Stakeholders (External Experts and other healthcare professionals within assigned geography/therapy area, investigators and potential investigators, and formulary decision makers) in a non-promotional manner and be responsive to unsolicited inquiries. Respond orally or by providing appropriate written materials to unsolicited requests for on- or off-label information or safety concerns that may have been asked of GSK sales staff or Medical and adhering to all policies and procedures regarding the provision of medical information. Gain valuable insight and feedback from the healthcare community on GSK products and services, medical and scientific information which can help guide research, development and service provision to benefit GSK’s customers and patients. Contribute in a manner that is always consistent with GSK Values and expectations demonstrating Courage, Accountability, Development, and Teamwork. Work with medical colleagues and other business partners to identify External Experts, professional groups, decision makers and other key stakeholders in the assigned therapy area and or geography. Attend and contribute (if required) to medical portion of regional account planning/training sessions. Maintain expertise in the evolving scientific / therapeutic area and in competitor medicines. Respond compliantly to unsolicited information requests from healthcare professionals and associated individuals regarding licensed or un-licensed GSK medicines and indications; ensure all medical information responses are factual, fair and balanced, scientifically rigorous and strictly comply with GSK standards and policies and with local codes of practice, guidelines and laws to ensure the strictest requirements are met. Disseminate important safety information to the healthcare profession as directed by the Medical Affairs or Research and Development teams or the Dear Healthcare Provider Letter (DHPL) process. Scientific exchange for a GSK medicine that is on label or consistent with the label to inform and educate HCPs on the appropriate use of our medicines in patients. Deliver scientific / pipeline presentations to formulary committees and HCPs per documented unsolicited request. Support clinical development activities and programs including GSK and Investigator sponsored studies as well as collaborating with R&D staff to improve site performance. Provide general insight into GSK research interests and field inquiries regarding investigator sponsored scientific or clinical research projects. Attend both national and regional scientific/medical meetings to gain medical voice of the customer on recent data being presented on products and disease states of interest to GSK. Conduct individual discussions and meetings with steering committee members, advisory board members, consultants etc., on topics related to the work being conducted with GSK (e.g. for clinical research investigators, the conduct or publication of clinical research sponsored by GSK). Provide scientific training for GSK sales representatives regarding GSK products and the conditions they treat utilizing approved Sales Training materials. Provide training to individual HCPs to prepare them to speak on behalf of GSK and assist with GSK-sponsored speaker training events. Partner with matrix colleagues (e.g. sales, marketing, market access, etc.) to ensure strategies and business plans are both patient and business focused and adding value to the external expert. Basic Qualifications: Pharm D, PhD, or M.D. A minimum of 2 years clinical practice and/or pharmaceutical industry experience. A minimum of two years’ experience applying knowledge of pharmacology and pharmacotherapy in humans in a clinical setting. Must live in designated territory and near a major airport. Must be willing to travel up to 70%. Preferred Qualifications: Hematology Oncology experience. Multiple Myeloma or Myleofibrosis experience. Nurse Practitioner or Physician Assistant with oncology background may be considered. Previous clinical experience in situations where direct/or indirect decision-making authority for patient care was demonstrated. At least one year of experience in pharmacology and pharmacotherapy in humans and applying this knowledge in a clinical setting. Above average computer literacy, including experience with software applications. Excellent interpersonal skills in both one on one and group settings. Proven ability to work autonomously and independently with time management skills to effectively manage field-based responsibilities. Strong communication skills: demonstrated ability to identify opportunities for medical engagement and develop a set of scientific engagement goals. Strong presentation skills. Preferred location with easy access to an airport that serves the states within assigned territory. Clear understanding of clinical research methodologies and a demonstrated ability to translate scientific, clinical and safety research studies in an effective credible manner. Ability to maintain a command of a large amount of scientific information across multiple products and show effective written/verbal communication skills. Ability to develop and maintain strong trusted relationships, with key decision makers. Demonstrated customer-focus, problem solving abilities and strong conflict resolution skills.
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