Medical Science Liaison-Cardiovascular - Texas

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

Region Covers: TX, TN, LA, AL, MS, AR, key markets include Dallas, Houston, Austin, New Orleans, Mobile, Birmingham, Jackson, Memphis, Nashville, Little Rock.

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. As an Amplity employee, we offer a comprehensive benefit package including medical, dental, vision, pet, 401K, company paid life insurance, long-term, short-term disability, mental wellness program, generous PTO, paid holidays and more.

The Medical Science Liaison (MSL) is responsible for providing scientific and clinical expertise to support clinical trial activities, fostering relationships with healthcare professionals (HCPs), clinical investigators, and key opinion leaders (KOLs), and serving as a bridge between clinical sites and internal teams. The MSL plays a critical role in ensuring the successful execution of clinical trials, patient enrollment, and compliance with industry regulations. This position requires extensive travel across assigned geographies to conduct site visits, support stakeholder engagement, and facilitate trial operations.

Employees can expect to be paid a salary of approximately $190K - $205K. The salary rage displayed may vary based on market data/ranges, an applicant's skills, prior relevant experience, certain degrees, certifications, and other relevant factors.

Essential Duties and Responsibilities:

1. Site Engagement and Support:

- 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.

2.Trial Facilitation:

- 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.

3.Stakeholder Management:

- 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.

4.Regulatory Compliance:

- Ensure all activities adhere to regulatory guidelines, company policies, and industry standards.

- Maintain documentation and reporting in compliance with organizational and regulatory requirements.

5.Data Management and Analysis:

- 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.

6.Networking and Industry Awareness:
- 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.

Required Knowledge, Skills, and Abilities:

• 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