Senior Medical Science Liaison (South Central)

Position OverviewConsidering making an application for this job Check all the details in this job description, and then click on Apply.The Senior Medical Science Liaison responsible for developing and expanding the clinical community's knowledge of the role for Minimal Residual Disease (MRD) in the management of lymphoid malignancies by educating and informing physicians about the clonoSEQ Assay.  Our MSL team will provide up-to-date medical information and education to local, regional, and national thought leaders related to use of the clonoSEQ Assay in hematological malignancies. Engagements include scientific exchange on relevant disease state(s) as well as the scientific advantage of NGS based MRD assessment.The Sr MSL role also includes developing creative and innovative tactics for addressing the specific needs of key customers; coordinate and manage regional investigator trials; represent real time voice of customer input related product development opportunities; conduct clinical presentations to payer organizations and patient advocacy groups. A minimum oversight is needed for Sr MSL role to drive above.Key Responsibilities and Essential FunctionsDevelop and maintain significant scientific relationships with hematology Key Opinion LeadersFocus to include educating physicians and other healthcare providers in the community oncology setting on disease state awareness, next generation sequencing minimal residual disease, and clinical utility through 1:1 discussions/presentations, roundtable discussions, or formal presentationsServe as a trusted clinical education/information subject matter expert to HCPs within academic and community institutions to help them better understand how MRD can be implemented in the patient's clinical journeyProvide internal teams with feedback and insights from interactions and discussions with HCPsCoordinate local and regional investigator initiated research (IIR)Manage IIR milestones and objectivesReport on scientific sessions at congressesRespond to and document unsolicited requests for scientific informationProvide clinical input and assist with training to internal functions as requestedProvide Advisory Board content development supportWork closely with other field-based teams and HQ staff to respond to information requests in a timely mannerAddress complex scientific/clinical topics and projects with minimal/no oversightPosition Requirements (Education, Experience, Other)RequiredMD, PharmD, or PhD preferred. Advanced professional degree (NP, PA, RPh, etc.) may be considered for candidates with significant clinical hematology/oncology experience.4+ years relevant industry and/or hematology/oncology disease experience required.2+ years MSL experience preferred.In-depth scientific and/or therapeutic knowledge required.Existing relationships with key opinion leaders and affiliated institutions required.Demonstrated understanding of clinical trial management.Working knowledge of regulatory guidance and reporting requirements.Exceptional organizational and time management skills.Strong presentations skills including excellent verbal and written communication.Strong interpersonal skills and demonstrated ability to work effectively in a cross functional team.A self-starter with a results-driven mentality and positive attitude.Computer proficiency in Excel, Word, PowerPoint, and Adobe.Working ConditionsAbility to travel up to >70% of the time#LI-RemoteCompensationSalary Range: $181,500 - $272,300Other compensation elements include:equity grantbonus eligibletransportation reimbursement#J-18808-Ljbffr

Created: 2024-11-06