Director, Clinical Trial Liaison

Jobtailor; Deutschland; Remote; EUR 90.000 - 130.000; Vollzeit

Zusammenfassung

Jobtailor is seeking a field-based investigator liaison to drive cardiovascular clinical trial operations in Germany. You will work directly with investigators and site staff to optimize recruitment, site feasibility, and study execution while traveling up to 70% to support trials across the region.

The role demands extensive CRO or industry experience in site-facing trials, strong communication, and a deep understanding of ICH/GCP.

Qualifikationen

• Bachelor's degree minimum; advanced degrees preferred (MD/PhD/PharmD).
• 10+ years in clinical research or CRO; site-facing trial operations experience.
• Cardiovascular clinical trial experience preferred.
• Fluency in English and local language; knowledge of ICH/GCP.
• Willingness to travel up to 70% and maintain regulatory/compliance standards.

Aufgaben

• Develop relationships with investigators and site staff to facilitate recruitment and trial execution.
• Support Global Development clinical study execution as the local field-based representative.
• Interact with investigator sites and other parties related to trial execution.
• Travel up to 70% to support site teams and troubleshoot challenges.
• Provide regional insights for site feasibility, selection, and recruitment strategies.
• Identify and resolve investigator site issues with study team.

Kenntnisse

Excellent communicator

Interpersonal skills

Cross-cultural awareness

Willingness to travel

Valid driver's license

Fluency in English

Ausbildung

Bachelor's degree

Master's or terminal degree (MD/PhD/PharmD)

Tools

Excel

Word

PowerPoint

Jobbeschreibung

• 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

Core Competencies

Demonstrates extensive experience in clinical trial operations, particularly in cardiovascular studies, with a strong ability to build relationships with investigators and site staff. Proficient in communicating complex scientific information and ensuring compliance with regulatory standards.

Highest-signal resume keywords

• Clinical Trial Operations
• Cardiovascular Clinical Trial Experience
• ICH/GCP Knowledge
• Excellent Communication Skills
• Fluency in English

ATS Optimization Keywords

Hard Skills

• Clinical Development Understanding
• Site Feasibility Assessment
• Patient Recruitment Strategy
• Data-Driven Insights
• Regulatory Compliance
• SOP Compliance
• Investigational Product Knowledge
• Enrollment and Retention Strategies
• Issue Resolution
• Site Selection

Soft Skills

• Interpersonal Skills
• Collaborative Working Style
• Proactive Attitude
• Organizational Skills
• Cross-Cultural Awareness

Industry Keywords

• Clinical Trials
• Investigational Agents
• Research Site Management
• Medical Affairs
• CRO Experience
• Cardiovascular Disease
• Regulatory GCP Inspections
• Study Team Collaboration
• Field-Based Representative
• Subject Recruitment

Tools & Technologies

• Excel
• Word
• PowerPoint