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Medical Science Liaison; Southeast Territory

Job in Orem, Utah County, Utah, 84057, USA
Listing for: Initial Therapeutics, Inc.
Full Time position
Listed on 2026-06-28
Job specializations:
  • Healthcare
    Clinical Research, Medical Science Liaison, Medical Science, Oncology
Salary/Wage Range or Industry Benchmark: 190000 - 205000 USD Yearly USD 190000.00 205000.00 YEAR
Job Description & How to Apply Below
Position: Medical Science Liaison (Southeast Territory)

MEDICAL SCIENCE LIAISON (SOUTHEAST TERRITORY)

Day One Biopharmaceuticals is an emerging, mission-driven, drug development company intentionally designed to identify, clinically evaluate, and successfully commercialize novel treatments for pediatric oncology patients, and ultimately to expand those benefits to patients of all ages. For more information, please visit our website at

POSITION SUMMARY:

The Medical Science Liaisons (MSLs) within Medical Affairs will have the overall responsibility of serving as a field-based extension of Day One Bio’s Medical Affairs and will represent the Company and our lead investigational compound Tovorafenib, currently being evaluated for treatment of pLGG and RAF-altered solid tumors. The MSL will provide scientific exchange, launch activities support, clinical trial and research support, KOL engagement and the support of ongoing development trials and pipeline products as requested.

The MSL will report into the National Director of Field Medical, Medical Affairs. The South Central MSL will be responsible for the territory including NC, SC, GA, AL, FL, and PR, which may be subject to some modification.

The MSL will build long term peer to peer relationships with researchers, thought leaders, and other stakeholders specializing in Pediatric Oncology treatment for the assigned region. The MSL will support Day One Bio’s clinical and research programs by delivering clinical, scientific, and technical education to the Pediatric Oncology community. This may expand to include the Adult Hematology/Oncology community and thought leaders.

The MSL is responsible for developing, coordinating, and assuring implementation of Day One Biopharmaceuticals’ corporate, scientific, and clinical strategies with thought leaders within academic, clinical, and healthcare organizations. Scientific exchanges will support and/or expand current therapeutic concepts, as well as ensure the safe and compliant utilization of Day One Bio product(s). Additionally, the MSL may support Day One Bio’s research initiatives including real world data generation, and investigator-sponsored trials (ISTs).

The MSL will have project and lead responsibilities in addition to the daily MSL role.

This position has the potential to be fully remote. Occasional travel will be required for in person meetings.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Establish Day One Bio as an innovative company committed to Pediatric oncology.
  • Maintain clinical, scientific, and technical expertise in relevant Pediatric Oncology tumors and other disease state areas as required, which may include some Adult Hematology/Oncology disease states.
  • Have a thorough understanding of pLGG and RAF-altered solid tumors (as well as other relevant disease states), drug development processes, clinical protocols, and related procedures.
  • Collaborate compliantly with medical affairs, clinical development, and other internal stakeholders, such as commercial and market access, and serve as a Day One Bio resource to HCPs, and large group medical practices when requested.
  • Develop and track key opinion leader (KOL) engagement plans – identify, develop and maintain long-term collaborative relationships with KOLs within assigned region. Participate in medical and scientific exchanges with the medical/scientific community including advisory boards and clinical trial sites.
  • Provide medical/clinical teams with feedback and insights from interactions with KOLs and investigators.
  • Respond in a timely manner to and document unsolicited requests for information on Day One Bio products and clinical programs.
  • Support internal requests for dossier review and medical review/consideration as requested.
  • Facilitate research collaborations and investigator sponsored trials (IST) with key investigators including helping to identify, establish, and maintain such collaborations.
  • Represent the company at medical meetings through Medical Affairs’ Scientific Booth coverage and other related activities.
  • Engage in speaker identification, training and evaluation and provide support for advisory board meetings as requested.
  • Collaborate and communicate with Market Access and Commercial…
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