Medical Science Liaison-Cardiovascular

About the position

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them. Medical Science Liaison-Cardiovascular Clinical Trial Focus California Region includes CA-San Jose, Los Angeles, San Diego, AZ, Phoenix, Tucson, NV, Las Vegas. We have an opportunity for an MSL/Clinical Trial Liaison as we build a new cardiovascular MSL team. This is a full-time salaried position with bonus potential and auto allowance.

Responsibilities

• Conduct regular site visits to establish and maintain collaborative relationships with clinical investigators, site staff, and HCPs.
• Provide scientific and clinical education to site teams to ensure understanding of study protocols, objectives, and procedures.
• Support clinical trial sites in overcoming challenges related to patient enrollment and adherence to study guidelines.
• Coordinate with internal teams to develop and implement strategies to enhance clinical trial participation and patient recruitment.
• Facilitate communication between clinical trial sites and internal stakeholders to ensure alignment and issue resolution.
• Monitor site performance and provide actionable insights to improve outcomes and engagement.
• Build and maintain effective relationships with KOLs, investigators, and other external stakeholders to support trial execution and scientific collaboration.
• Present scientific data and clinical trial information to stakeholders through formal presentations and meetings.
• Ensure all activities adhere to regulatory guidelines, company policies, and industry standards.
• Maintain documentation and reporting in compliance with organizational and regulatory requirements.
• Utilize data management tools and analysis software to track site metrics and performance.
• Identify trends, opportunities, and challenges through data analysis to inform decision-making and strategic planning.
• Stay abreast of industry trends, scientific advancements, and regulatory changes to inform clinical trial strategies.
• Represent the organization at industry events, conferences, and meetings as needed.

Requirements

• PharmD, Ph.D. NP, PA, or other medical credentials with relevant clinical experience.
• Strong communication and interpersonal skills to build rapport with diverse audiences.
• Pharmaceutical industry experience needed.
• Clinical trial experience required.
• MSL/MSL like/Medical Affairs experience.
• Cardiovascular experience highly preferred.
• Exceptional organizational skills and attention to detail, with the ability to manage multiple tasks and projects simultaneously.
• Proficiency in data management and analysis tools, along with standard office software (e.g., Microsoft Office Suite).
• Ability to work independently and collaboratively in a team environment across large geographies.
• Experienced presenter with a proven ability to conduct engaging and informative meetings.
• Effective networking skills to build and maintain relationships with clinical site investigators and KOLs.
• Compliance-focused mindset with the ability to work in a highly regulated environment.
• High learning agility and clinical acumen to quickly adapt to scientific and industry advancements.
• Demonstrates integrity, a strong work ethic, and flexibility in the face of change.

Benefits

• Comprehensive benefit package including medical, dental, vision, pet insurance.
• 401K.
• Company paid life insurance.
• Long-term and short-term disability.
• Mental wellness program.
• Generous PTO.
• Paid holidays.