Rare Disease Medical Science Liaison- South Central
$170,000–$195,000 year
On-siteDallas, Texas, United States
Job Summary
Establish and maintain strategic scientific relationships with key opinion leaders, healthcare professionals, and investigators across Dallas, Houston, and Phoenix territories. Serve as the regional scientific expert by engaging in compliant, peer-to-peer scientific exchanges, gathering actionable medical insights, and supporting evidence generation for Kyowa Kirin's rare disease therapeutic areas. Deliver scientific presentations and educational programs to external stakeholders while building cross-functional partnerships with Clinical Development, Commercial, and Regulatory Affairs teams. This field-based position requires up to 70% travel by air and ground, including overnight commitments to support scientific congresses and advisory boards. Candidates must reside within the assigned territory and hold a valid driver's license. The role offers a salary range of $170,000 – $195,000 and includes comprehensive benefits such as 401K matching, annual bonuses, and extensive PTO.
Required Qualifications
- Advanced clinical or scientific degree or healthcare professional credential (MD, DO, PhD, PharmD, NP, PA, MS, or equivalent)
- Minimum of two (2) years of experience as a Medical Science Liaison (MSL), field-based medical professional, or in a related clinical, scientific, or Medical Affairs role
- Background in the Rare-Disease therapeutic area or related disease state
- Demonstrated ability to engage healthcare professionals (HCPs), key opinion leaders (KOLs), investigators, and other external stakeholders through compliant scientific exchange
- Ability to interpret and communicate clinical and scientific data effectively to diverse audiences
- Familiarity with clinical research activities, including investigator-initiated studies (IIS) and/or company-sponsored clinical trials
- Involvement in scientific congresses, advisory boards, investigator meetings, or other medical education activities
- Understanding of assigned disease states, therapeutic landscapes, treatment guidelines, and current standards of care
- Familiarity with clinical research methodology, evidence generation strategies, and interpretation of clinical trial data
- Working knowledge of FDA regulations, Good Clinical Practice (GCP), pharmacovigilance requirements, Office of Inspector General (OIG) guidance, and applicable industry standards
- Proficiency in evaluating medical literature, synthesizing scientific information, and translating complex data into meaningful insights for healthcare professionals and internal stakeholders
- Skilled in delivering scientifically accurate, balanced, and compliant presentations to external and internal audiences
- Experience utilizing Medical Affairs systems, customer relationship management (CRM) platforms, and proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)
- Demonstrated capability to analyze medical insights, identify trends, and support data-driven decision-making within Medical Affairs
- Capacity to manage multiple priorities, organize field-based activities, and operate effectively in a dynamic, cross-functional environment
- Outstanding interpersonal skills, including the ability to build strong working relationships and effectively manage conflict
- Ability to thrive in a fast-paced environment while managing ambiguity effectively
- Commitment to the highest ethical, legal, regulatory, and scientific standards
- Demonstrated professionalism, sound judgment, and scientific integrity
- Passion for personal learning and professional development
- Cultural sensitivity and adaptability within multinational organizations
- Valid driver's license and the ability to operate a motor vehicle as required for business travel
- Must reside within the assigned territory (Dallas, TX, Houston, TX, and Phoenix, AZ) and maintain proximity to a major airport
Desired Qualifications
- Doctoral degree (MD, DO, PhD, or PharmD)
- Experience in a related clinical, scientific, or Medical Affairs role (in addition to the 2 years required)
- Familiarity with clinical research activities, including investigator-initiated studies (IIS) and/or company-sponsored clinical trials
- Involvement in scientific congresses, advisory boards, investigator meetings, or other medical education activities
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.