Position Overview

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 Functions

• Develop and maintain significant scientific relationships with hematology Key Opinion Leaders
• Focus 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 presentations
• Serve 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 journey
• Provide internal teams with feedback and insights from interactions and discussions with HCPs
• Coordinate local and regional investigator initiated research (IIR)
• Manage IIR milestones and objectives
• Report on scientific sessions at congresses
• Respond to and document unsolicited requests for scientific information
• Provide clinical input and assist with training to internal functions as requested
• Work closely with other field-based teams and HQ staff to respond to information requests in a timely manner
• Address complex scientific/clinical topics and projects with minimal/no oversight

Position Requirements (Education, Experience, Other)

Required

• MD, 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.
• 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.

• Existing relationships with key opinion leaders and affiliated institutions preferred. 

   

Working Conditions

Ability to travel up to >70% of the time

Compensation

Salary Range: $179,800 - $269,600

Possible "other compensation" elements to include:

• equity grant
• bonus eligible
• transportation reimbursement