Medical Science Liaison, Obesity

Viking Therapeutics, Inc.

. Develop and execute territory plans engaging key opinion leaders, clinical investigators, centers of excellence, health systems, and professional societies .

Posted 11/6/2026full-timeRemote • California • United StatesMid-LevelSenior💰 $180,000 - $210,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates advanced scientific knowledge in obesity and cardiometabolic diseases, with the ability to engage healthcare professionals and deliver evidence-based presentations. Proficient in clinical trial processes and compliance requirements, while effectively collaborating with cross-functional teams to inform medical strategy.

Highest-signal resume keywords

Advanced Doctoral DegreeMSL ExperienceScientific Presentation SkillsClinical Trial ProcessesTerritory Planning

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Scientific Knowledge of ObesityClinical Data EvaluationEvidence Gap IdentificationMedical Strategy ContributionField Insights Synthesis

Soft Skills

Interpersonal SkillsOrganizational SkillsTime Management Skills

Tools & Technologies

CRM Systems

Certifications & Qualifications

Valid Driver's License

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryClinical ResearchHealth SystemsCompliance Requirements

About the role

Key responsibilities & impact

Develop and execute territory plans engaging key opinion leaders, clinical investigators, centers of excellence, health systems, and professional societies
Establish and maintain peer-to-peer relationships with external experts and healthcare professionals
Deliver scientifically balanced, evidence-based presentations
Respond to unsolicited medical information requests in compliance with company policy and regulations
Identify healthcare professional educational needs and provide tailored scientific content
Support clinical trial site identification, feasibility assessment, and investigator engagement
Provide scientific support to active and prospective trial sites and facilitate communication with Clinical Operations
Gather and synthesize field insights on clinical practice, treatment paradigms, unmet needs, and competitive landscape
Identify evidence gaps and contribute to medical strategy and publication planning
Collaborate with Clinical Development, Regulatory, Medical Information, and other cross-functional partners
Serve as a scientific resource at medical congresses, advisory boards, roundtables, and investigator meetings
Support external expert identification and speaker training
Participate in MSL strategy, training, and operations project teams
Contribute to field medical metrics, dashboards, and SOPs
Document field interactions and insights in the assigned CRM or system
Complete required training and administrative tasks on time
Remain current on emerging literature, treatment guidelines, and competitive landscape
Ensure activities comply with applicable laws, regulations, industry codes, and Viking policies

Requirements

What you’ll need

Advanced doctoral degree in life or clinical sciences (Pharm.D., Ph.D., M.D., D.O., or equivalent); nurse practitioner or physician assistant degrees will be considered
At least 3 years of experience in the pharmaceutical or biotechnology industry, a health system, or a related clinical research setting
Prior MSL experience strongly preferred
Deep scientific knowledge of obesity, endocrinology, metabolism, or a related therapeutic area
Established relationships within the obesity and cardiometabolic medical community preferred
Strong understanding of obesity and cardiometabolic disease, including treatment approaches, emerging therapies, and relevant scientific literature
Ability to critically evaluate clinical data and communicate complex scientific information clearly to diverse healthcare audiences
Excellent scientific presentation and interpersonal skills
Knowledge of clinical trial processes, including site identification, feasibility assessment, and investigator engagement
Understanding of compliance requirements governing scientific exchange, medical information responses, and field medical activities
Ability to gather and synthesize field insights, identify evidence gaps, and communicate findings to inform medical strategy
Strong territory planning, organizational, and time management skills
Ability to collaborate effectively with Medical Affairs, Clinical Development, Clinical Operations, Regulatory, and other cross-functional teams
Proficiency in CRM systems and accurate, timely documentation of field interactions and insights
Valid driver's license
Ability to travel 50–75%, primarily within the assigned territory, by car and air