TalentBurst
Overview
Medical Science Liaison III Medical Science Liaison position based in Research Triangle Park, NC 27709. Duration: 12 Months (Possible Extension). Remote work available – candidates should be based in the western US. Description: The Medical Science Liaison (MSL) is a field-based scientific resource that strategically and tactically supports the development, medical, and scientific objectives of AskBio’s gene therapy portfolio/pipeline across its development phases. The MSL will work closely with the Sr Director Medical Affairs CNS Therapeutic Area Lead, the Field Medical Advisor Gene Therapy (FMAGT), and the Clinical Operations & Clinical Development teams to help ensure successful clinical trials from early feasibility to study completion. The MSL will act as a peer scientific guide who communicates accurate scientific and medical information to Principal/Sub-Investigators and Key Opinion Leaders (KOLs) and collects relevant field data. The MSL reports to the Sr Director Medical Affairs – Therapeutic Area Lead CNS. This role aligns medical affairs with clinical development, medical communications, field engagement, and evidence generation to support medical excellence from early development through commercialization. Responsibilities
Clinical Trial Support
Develop, maintain, manage, and link relationships within investigational sites and across relevant referral networks to increase awareness of the clinical trial and maximize enrollment goals. Drive identification of potential sites and investigators for clinical trials. In collaboration with Clinical Development and Operations teams, support clinical study feasibility and effective study implementation. Enhance clinical operations efforts to support and/or improve recruitment & retention through education, training, and clinical discussions with the clinical research/investigator team. Support development of patient referral networks within the geographic area. Identify effective prescreening strategies for each trial and recommend improvements. Work with the study team to develop, plan, and execute strategies to increase enrollment at the clinical trial site level. Support the Development CNS Center Of Excellence Map considering criteria including KOLs/TLs, geographic footprint, referral network, capacity, and infrastructure. External Engagement & Development
Establish a network of KOLs focused on clinical management of conditions in AskBio’s therapeutic areas of interest. Identify new KOL/HCPs for future engagement, including clinical researchers, scientific advisors, and medical educators. Collect medical insights and intelligence from scientific exchanges with clinical investigators and thought leaders. Attend and support key Medical/Scientific meetings to establish contacts, evaluate the field, and identify improvements in trial design, conduct, and patient recruitment/retention initiatives. Support Therapeutic Area Scientific/Clinical National and Regional Advisory Board meetings as required. Collaborate with the Director Patient Advocacy and Sr Director Medical Affairs and Therapeutic Area Lead to support Patient Advocacy initiatives aligned with programs and product strategies. Cross-functionally identify feasibility and interest of investigators for Investigator Initiated Studies (IIS) aligned with the asset and pipeline. Scientific/Medical Communication
Develop and maintain the highest scientific and medical expertise in the relevant fields and be recognized as an internal and external expert and resource in the assigned therapeutic area. Identify educational opportunities within the assigned geography and address gaps by delivering educational presentations to external audiences, stakeholders, and customer groups. Provide timely, accurate, specific, and balanced responses to Medical Inquiries in collaboration with the Sr Director Medical Affairs and Therapeutic Area Lead. Compliance
Stay current on local laws and guidelines, codes of practice, and AskBio policies relevant to Clinical Development and Medical Affairs activities. Adhere to SOPs and FDA guidance for distribution of scientific information and to compliance guidelines for all external contacts. Qualifications and experience
Advanced Degree (M.D./Ph.D./ Pharm.D.) in Medicine and/or a medical sciences field is required; preferably in CNS/Neuroscience/metabolic disorders; Minimum 5 years of combined experience in Medical Affairs/Clinical Operations/Clinical Development; Previous career experience as a field-based Medical Affairs representative or MSL; Experience collaborating with medical staff in both office and hospital-based clinical trials; Prior experience in gene therapy is advantageous; Ability to plan, prioritize, and execute multiple projects; multitask and work independently and with cross-functional teams; Ability to communicate the scientific basis of trials to team members, investigators, and site staff; Independently motivated working style with strong problem-solving skills and ability to analyze, synthesize, and compile data from diverse disciplines; Strong interpersonal skills for effective communications with internal and external stakeholders; Excellent presentation and computer skills (Word, Excel, PowerPoint); Highly motivated team player; Ability to travel to meetings/conferences up to 50% of the time. #TB_PH
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Medical Science Liaison III Medical Science Liaison position based in Research Triangle Park, NC 27709. Duration: 12 Months (Possible Extension). Remote work available – candidates should be based in the western US. Description: The Medical Science Liaison (MSL) is a field-based scientific resource that strategically and tactically supports the development, medical, and scientific objectives of AskBio’s gene therapy portfolio/pipeline across its development phases. The MSL will work closely with the Sr Director Medical Affairs CNS Therapeutic Area Lead, the Field Medical Advisor Gene Therapy (FMAGT), and the Clinical Operations & Clinical Development teams to help ensure successful clinical trials from early feasibility to study completion. The MSL will act as a peer scientific guide who communicates accurate scientific and medical information to Principal/Sub-Investigators and Key Opinion Leaders (KOLs) and collects relevant field data. The MSL reports to the Sr Director Medical Affairs – Therapeutic Area Lead CNS. This role aligns medical affairs with clinical development, medical communications, field engagement, and evidence generation to support medical excellence from early development through commercialization. Responsibilities
Clinical Trial Support
Develop, maintain, manage, and link relationships within investigational sites and across relevant referral networks to increase awareness of the clinical trial and maximize enrollment goals. Drive identification of potential sites and investigators for clinical trials. In collaboration with Clinical Development and Operations teams, support clinical study feasibility and effective study implementation. Enhance clinical operations efforts to support and/or improve recruitment & retention through education, training, and clinical discussions with the clinical research/investigator team. Support development of patient referral networks within the geographic area. Identify effective prescreening strategies for each trial and recommend improvements. Work with the study team to develop, plan, and execute strategies to increase enrollment at the clinical trial site level. Support the Development CNS Center Of Excellence Map considering criteria including KOLs/TLs, geographic footprint, referral network, capacity, and infrastructure. External Engagement & Development
Establish a network of KOLs focused on clinical management of conditions in AskBio’s therapeutic areas of interest. Identify new KOL/HCPs for future engagement, including clinical researchers, scientific advisors, and medical educators. Collect medical insights and intelligence from scientific exchanges with clinical investigators and thought leaders. Attend and support key Medical/Scientific meetings to establish contacts, evaluate the field, and identify improvements in trial design, conduct, and patient recruitment/retention initiatives. Support Therapeutic Area Scientific/Clinical National and Regional Advisory Board meetings as required. Collaborate with the Director Patient Advocacy and Sr Director Medical Affairs and Therapeutic Area Lead to support Patient Advocacy initiatives aligned with programs and product strategies. Cross-functionally identify feasibility and interest of investigators for Investigator Initiated Studies (IIS) aligned with the asset and pipeline. Scientific/Medical Communication
Develop and maintain the highest scientific and medical expertise in the relevant fields and be recognized as an internal and external expert and resource in the assigned therapeutic area. Identify educational opportunities within the assigned geography and address gaps by delivering educational presentations to external audiences, stakeholders, and customer groups. Provide timely, accurate, specific, and balanced responses to Medical Inquiries in collaboration with the Sr Director Medical Affairs and Therapeutic Area Lead. Compliance
Stay current on local laws and guidelines, codes of practice, and AskBio policies relevant to Clinical Development and Medical Affairs activities. Adhere to SOPs and FDA guidance for distribution of scientific information and to compliance guidelines for all external contacts. Qualifications and experience
Advanced Degree (M.D./Ph.D./ Pharm.D.) in Medicine and/or a medical sciences field is required; preferably in CNS/Neuroscience/metabolic disorders; Minimum 5 years of combined experience in Medical Affairs/Clinical Operations/Clinical Development; Previous career experience as a field-based Medical Affairs representative or MSL; Experience collaborating with medical staff in both office and hospital-based clinical trials; Prior experience in gene therapy is advantageous; Ability to plan, prioritize, and execute multiple projects; multitask and work independently and with cross-functional teams; Ability to communicate the scientific basis of trials to team members, investigators, and site staff; Independently motivated working style with strong problem-solving skills and ability to analyze, synthesize, and compile data from diverse disciplines; Strong interpersonal skills for effective communications with internal and external stakeholders; Excellent presentation and computer skills (Word, Excel, PowerPoint); Highly motivated team player; Ability to travel to meetings/conferences up to 50% of the time. #TB_PH
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