BESTMSLs, a Uniphar company
Medical Science Liaison, Hematology/Oncology (Colorado Territory)
BESTMSLs, a Uniphar company, Denver, Colorado, United States, 80285
Medical Science Liaison, Hematology/Oncology (Central Territory)
Overview: The Medical Science Liaison (MSL) will serve as the field‑based scientific expert whose mission is to foster collaborative relationships with opinion leaders focused on a rare hematologic disorder and to facilitate the exchange of unbiased scientific information between the medical community and the company. The MSL will have clinical/medical affairs expertise to serve as a peer‑to‑peer liaison internally and externally. This role will cover the Central territory: Colorado, Nebraska, Kansas, Oklahoma, Missouri, Arkansas, and Louisiana. Responsibilities
Deliver clinical and scientific presentations to health care professionals, including clinicians and P&T committee members. Provide scientific support at medical conferences and support the medical community with up‑to‑date medical information, disease expertise, and product information for the rare hematologic disorder. Maintain peer‑to‑peer collaborations and relationships with key medical experts in relevant therapeutic areas. Respond to unsolicited medical information requests using a customized approach. Collaborate with physicians on medical affairs initiatives, including assistance with publications and investigator‑initiated trials, as well as company‑sponsored research. Support clinical initiatives, including assessment and selection of clinical investigations, site identification, registry and presentation of final approved data. Provide medical and scientific input into the planning and execution of advisory boards; work with physician experts to review speaker presentations and provide medical references when requested. Train staff, including the sales team, on key scientific and medical topics in relevant therapeutic areas. Participate in the development and review of professional slide decks, medical letters, and clinical summaries. Develop territory plan with input from direct line manager. Gather and share clinical field insights with the team on a regular basis. Act in full compliance with all laws, regulations, and policies, including adverse event and pharmacovigilance responsibilities. Perform additional duties as assigned. Qualifications
Advanced scientific degree (MD, DO, PhD, PharmD) in medical or biological sciences. Minimum of two years of experience in medical affairs or clinical functions (strongly preferred). Familiarity with drug development process, FDA, ICH, and GCP guidelines. Experience implementing, monitoring, or managing clinical trials for academic or pharmaceutical/biotechnology research (a plus). Knowledge and Skills
Ability to review and interpret clinical data. Ability to develop clinical data and medical content for internal and external audiences. Proficiency in Microsoft Office (Word, PowerPoint, Excel). Strong presentation and communication skills. Project management experience (a plus). Experience with rare diseases (a plus). Excellent time management and ability to work independently. Excellent written and verbal communication skills. Location / Travel
Field‑based position, must be near a major airport and based within the Central territory. Approximately 60% travel required within Colorado, Nebraska, Kansas, Oklahoma, Missouri, Arkansas, and Louisiana. Employment Type
Full‑time, Entry level.
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Overview: The Medical Science Liaison (MSL) will serve as the field‑based scientific expert whose mission is to foster collaborative relationships with opinion leaders focused on a rare hematologic disorder and to facilitate the exchange of unbiased scientific information between the medical community and the company. The MSL will have clinical/medical affairs expertise to serve as a peer‑to‑peer liaison internally and externally. This role will cover the Central territory: Colorado, Nebraska, Kansas, Oklahoma, Missouri, Arkansas, and Louisiana. Responsibilities
Deliver clinical and scientific presentations to health care professionals, including clinicians and P&T committee members. Provide scientific support at medical conferences and support the medical community with up‑to‑date medical information, disease expertise, and product information for the rare hematologic disorder. Maintain peer‑to‑peer collaborations and relationships with key medical experts in relevant therapeutic areas. Respond to unsolicited medical information requests using a customized approach. Collaborate with physicians on medical affairs initiatives, including assistance with publications and investigator‑initiated trials, as well as company‑sponsored research. Support clinical initiatives, including assessment and selection of clinical investigations, site identification, registry and presentation of final approved data. Provide medical and scientific input into the planning and execution of advisory boards; work with physician experts to review speaker presentations and provide medical references when requested. Train staff, including the sales team, on key scientific and medical topics in relevant therapeutic areas. Participate in the development and review of professional slide decks, medical letters, and clinical summaries. Develop territory plan with input from direct line manager. Gather and share clinical field insights with the team on a regular basis. Act in full compliance with all laws, regulations, and policies, including adverse event and pharmacovigilance responsibilities. Perform additional duties as assigned. Qualifications
Advanced scientific degree (MD, DO, PhD, PharmD) in medical or biological sciences. Minimum of two years of experience in medical affairs or clinical functions (strongly preferred). Familiarity with drug development process, FDA, ICH, and GCP guidelines. Experience implementing, monitoring, or managing clinical trials for academic or pharmaceutical/biotechnology research (a plus). Knowledge and Skills
Ability to review and interpret clinical data. Ability to develop clinical data and medical content for internal and external audiences. Proficiency in Microsoft Office (Word, PowerPoint, Excel). Strong presentation and communication skills. Project management experience (a plus). Experience with rare diseases (a plus). Excellent time management and ability to work independently. Excellent written and verbal communication skills. Location / Travel
Field‑based position, must be near a major airport and based within the Central territory. Approximately 60% travel required within Colorado, Nebraska, Kansas, Oklahoma, Missouri, Arkansas, and Louisiana. Employment Type
Full‑time, Entry level.
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