Director, Clinical Trial Liaison

🔥 12 hours ago

🇺🇸 United States – Remote

💵 $253k - $329k / year

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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Kardigan

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2023

🏥 Healthcare

💼 Consulting

🎖️ Defense

Healthcare • Consulting • Defense

Kardigan is a heart health company dedicated to reimagining cardiovascular medicine. The company is focused on making cardiovascular disease preventable and curable, actively developing multiple targeted treatments to improve patient outcomes. Kardigan utilizes a cutting-edge research platform and is led by an experienced team with a deep background in cardiovascular drug development. Their mission is to innovate and accelerate the creation of medicines that directly address the underlying causes of cardiovascular diseases, transitioning from traditional symptom management to functional cures.

📋 Description

• Develop relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in Kardigan clinical trials • Support Global Development clinical study execution as the local field-based representative • Interact with investigator sites and other parties related to clinical trial execution • Travel up to 70% as needed to support site teams, troubleshoot challenges, and foster collaborative relationships • Provide regional and country-specific insights for study feasibility, site identification and selection, and patient recruitment and retention • Identify and help resolve investigator site issues with the study team • Ensure investigators and site staff understand investigational agents, eligibility criteria, and study procedures • Assess site strategies for identifying eligible subjects and understand competing trials or upcoming approvals affecting recruitment • Liaise with key investigators and transmit site queries or concerns to the sponsor • Provide regional operational insight into site feasibility, selection, and patient recruitment strategy • Identify and cultivate high-quality cardiovascular investigators • Communicate scientific and clinical information, including study objectives, rationale, investigational product profiles, and updates • Collaborate with Clinical Operations, Clinical Development, Medical Affairs, Clinical Operations, and other cross-functional stakeholders • Participate in study team and quality meetings, SIVs, investigator meetings, monitor workshops, and training • Conduct or participate in site visits and report feasibility, startup, enrollment, and escalated site issues • Support enrollment and retention through tailored discussions, data-driven insights, and relationship-building • Review, document, follow up, and track investigator site issues and metrics • Serve as sponsor regional operational support and escalation point for investigator sites • Participate in Regulatory GCP inspections and/or audits as sponsor representative • Complete SOP-compliant training, field activity documentation, expense reporting, and assigned administrative tasks • Support educational materials and communicate trial science to team members, investigators, and site staff • Identify prescreening strategies and recommend improvements • Provide detailed reports of investigator and site staff interactions • Ensure interactions comply with regulatory, ethical, and company standards

🎯 Requirements

• Minimum Bachelor’s degree; master’s preferred or terminal degree (MD, PhD or PharmD) • 10+ years relevant industry and/or CRO experience required • Extensive experience in site facing clinical trial operations required • Cardiovascular clinical trial experience and expertise in cardiovascular disease preferred • Extensive medical and scientific knowledge and clinical development understanding • Excellent communicator of technical and scientific information • Excellent interpersonal skills and demonstrated collaborative as well as independent working style • Ability to build relations with the external medical community • Proactive and self-motivated, with ability to align activities with clinical development plans (CDPs) • Strong organizational skills with effective use of time and prioritization • Cross-cultural awareness • Fluency in English and in the local language in country of residence required • Working knowledge of ICH/GCP • Computer skills including Excel, Word, and PowerPoint • Willingness to travel frequently within assigned geographical territory, including overnight travel • Valid driver’s license