Medical Science Liaison - West
Full Time
full-time
$200,000 - $265,000/year
1 Nov 2025
Los Angeles Metropolitan Area
Verified by Turrior
Content + Source + Freshness • 17 Dec 2025 • 95% confidence
88 / 100
Offer value
Strong opportunity with high compensation, influential networking in the medical community, and engagement in critical clinical research.
- Excellent salary: $200,000–$265,000/year
- Influential role in clinical research
- Opportunities for professional networking
- Demands high experience and commitment
Pros
- Salary range ($200,000–$265,000/year) is very competitive
- Engagement with esteemed medical professionals enhances networking
- Vital role in clinical development and research processes
Cons
- Heavy workload with potential for long hours
- Position may involve frequent travel
- Requires advanced knowledge and experience in medical science
Who it's for
Senior • Full-time, On-site
Good fit
- Senior medical professionals with extensive experience
- Individuals with a strong interest in clinical research
- Networking-oriented candidates
Not recommended for
- New graduates or entry-level professionals
- Individuals seeking a standard work schedule
- Those unable to travel frequently
Motivation fit
Desire to work at the intersection of science and clinical applicationInterest in influencing the medical landscapeWillingness to engage in challenging environments with high stakes
Key skills
Clinical research knowledgeStrong communication and networkingUnderstanding of medical regulationsStakeholder engagement
Score: 88/100 AI verified analysis
About the job
IQVIA is seeking a Medical Science Liaison - West to join their team in the Los Angeles Metropolitan Area. The role involves facilitating relationships with the medical/scientific community and providing field-based medical support to clinical research programs.As a Medical Science Liaison, you will be responsible for engaging with clinical trial site investigators, delivering presentations on scientific matters, and supporting clinical development teams. You will also report field intelligence, maintain relationships with site management, and ensure compliance with laws and regulations while facilitating clinical trials.
