Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Galderma

Medical Science Liaison

Galderma

. Serve as an internal expert supporting the U.S.

Posted 9/21/2026full-timeUnited StatesMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Medical Science Liaison activities, with a strong focus on building relationships with healthcare professionals and delivering scientific information about Nemolizumab. Possesses a solid understanding of regulatory compliance and the ability to execute medical affairs strategies effectively.

Highest-signal resume keywords
Pharm.D.Ph.D.MDMedical Affairs ExperienceDermatology Background

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical ResearchMedical ResearchScientific CommunicationData GenerationKOL EngagementDisease Awareness ActivitiesRegulatory ComplianceMetrics ExecutionTraining DevelopmentPresentation Skills
Soft Skills
Relationship BuildingTime ManagementOrganizational SkillsCredibility with Medical ProfessionalsEffective Communication
Tools & Technologies
Technical PlatformsCompliance Guidelines
Industry Keywords
FDA RegulationsOIG GuidelinesHIPAA ComplianceAtopic DermatitisPrurigo NodularisBiologicsClinical AcumenBusiness AcumenHealthcare ProvidersAdvisory Board Planning

About the role

Key responsibilities & impact
  • Serve as an internal expert supporting the U.S. Nemolizumab team
  • Develop and maintain professional relationships with physicians, healthcare providers, nurse practitioners, physician assistants, clinical investigators, and professional organizations
  • Provide proactive and reactive scientific information about Nemolizumab in a compliant manner
  • Identify key opinion leaders and cultivate a network of experts
  • Prepare and execute KOL engagement plans and maintain US KOL and institution plans
  • Collaborate with healthcare professionals on algorithms and guidelines
  • Execute qualitative and quantitative metrics required by the US medical affairs strategy
  • Gather and communicate medical insights and feedback to support medical affairs strategies
  • Conduct disease-awareness activities and educate healthcare providers on disease-state concepts
  • Provide drug, mechanism-of-action, and emerging clinical information to healthcare providers
  • Support patient groups, educational foundations, disease-state advocacy groups, and professional organizations
  • Identify research gaps and facilitate data-generation opportunities, including posthoc analyses, IITs, and Medical Affairs-sponsored studies
  • Attend scientific congresses, engage external stakeholders, prepare congress summaries, and present perspectives to internal stakeholders
  • Maintain current knowledge of atopic dermatitis and prurigo nodularis through scientific literature review
  • Develop and conduct external and internal trainings and continuing education
  • Ensure stakeholder activities comply with legal and compliance guidelines
  • Support advisory-board planning and execution and review physician speaker presentations
  • Territory includes NC, SC, GA, and TN

Requirements

What you’ll need
  • Pharm.D., Ph.D., or MD required
  • Doctorate degree and 1–2 years of MSL/Medical Affairs experience preferred
  • Three (3) plus years of clinical practice, clinical research, or medical research preferred
  • Post-doctoral training, including residencies and/or fellowships, may count as medically related experience
  • Dermatology or Immunology background preferred
  • Biologic and/or launch experience preferred
  • Excellent communication, presentation, and time management skills required
  • Ability to interface effectively with a variety of technical platforms
  • Solid understanding of FDA, OIG, HIPAA, and other US regulatory principles
  • Current working knowledge of US legal, regulatory, and compliance regulations and guidelines
  • Strong scientific and/or clinical acumen
  • Strong business acumen
  • Ability to organize, prioritize, and work effectively with a sense of urgency in an evolving environment
  • Demonstrated credibility with medical professionals and ability to develop good relationships
  • Ability to complete expense reports in a compliant and timely manner
  • Ability to manage travel in an organized and effective manner
  • Travel estimated at 70–80%

Benefits

Comp & perks
  • Annual short-term incentive program based on corporate performance with a multiplier focused on individual performance
  • Health insurance
  • 401(k) plan with employer match
  • Generous paid time off policy
  • Hybrid work schedules
  • Diversity and inclusion-focused workplace