Medical Science Liaison Clinical Trials

Medical Science Liaison

We are excited to announce that currently we are looking for a Medical Science Liaison with experience in viral liver disease, hepatology, Infectious Disease/HIV to initiate scientific dialogue within the therapeutic area centers through scientific discussions with clinical physicians, staff and other stakeholders, on behalf of our client. In addition, you will ensure compliant and high-quality clinical scientific communication. Pre-launch medical readiness through HDV territory uncovering, ecosystem mapping, scientific relationship building, and actionable insight generation. The Medical Science Liaison (MSL) is a field-based scientific role responsible for advancing pre-launch medical readiness for hepatitis delta virus (HDV) across the US Central territory. build and advance credible peer-to-peer scientific relationships with healthcare professionals (HCPs), investigators, and key opinion leaders (KOLs); The primary objective of the role is to expand Vir Bio's medical footprint and support future launch readiness through systematic territory uncovering, compliant scientific engagement, relationship development, and the collection and timely sharing of high-quality, actionable field insights. The role will engage beyond clinical trial sites to identify the clinicians, centres, networks, and local dynamics that shape HDV awareness, screening, diagnosis, referral, and treatment readiness.

ECLIPSE clinical trial support will remain within scope, with a focus on maintaining the scientific relationship with Rush University Medical Center, supporting the Principal Investigator and site stakeholders as appropriate, and contributing to participant retention and study execution within compliant MSL boundaries. Territory and Travel:

Extensive travel throughout the territory is expected to support in-person scientific engagement, relationship development, congress participation, and territory mapping.

Scientific engagement and relationship management

Insight generation and medical intelligence

Cross-functional collaboration and scientific leadership

Priorities and responsibilities may evolve in line with the medical strategy, clinical programme, and stage of product development.

An advanced clinical, medical, or scientific degree, such as a PharmD, MD, PhD, or relevant master's degree, is required.

Demonstrated experience conducting credible, compliant peer-to-peer scientific exchange with HCPs and KOLs.

Valid driver's license and ability to travel extensively within the territory, including overnight travel.

Travel of up to 70% may be required.

Therapeutic area experience in viral hepatitis, hepatology, infectious diseases, gastroenterology, or a closely related field is strongly preferred.

Experience with territory planning, KOL mapping, ecosystem mapping, relationship development, and actionable insight generation.

Clinical trial experience and experience collaborating with investigators, site teams, and Clinical Operations are preferred.

Ability to work autonomously across a broad geography, prioritize strategically, and translate field information into clear actions and recommendations.

Knowledge of applicable guidelines and requirements for compliant scientific communication and the US regulatory environment.

Proficiency with CRM systems and standard collaboration tools, including Microsoft Teams, SharePoint, PowerPoint, Outlook, and Power BI or similar reporting tools.

Excellent written and oral communication, presentation, relationship-building, and organizational skills.

A self-directed, field-oriented medical professional who is comfortable building a territory and creating new scientific relationships.

Strong scientific curiosity and the ability to uncover meaningful information through thoughtful, compliant questioning and active listening.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.