Clinical Trial Liaison

Jazz Pharmaceuticals

. Build peer-to-peer relationships with Principal Investigators and site staff in Neuroscience and Oncology .

Posted 10/30/2026full-timeRemote • United StatesMid-LevelSenior💰 $121,600 - $182,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Oncology and Neuroscience with a strong understanding of clinical trial methodology, regulatory requirements, and the ability to build relationships with healthcare professionals and key opinion leaders. Proven skills in strategic planning, communication, and collaboration to enhance site engagement and operational performance.

Highest-signal resume keywords

Advanced Degree (PharmD, MD, PhD)Medical Scientific Liaison (MSL) ExperienceClinical Trial Methodology KnowledgeStrong Communication SkillsInterpersonal Relationship Building

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Oncology MedicineNeuroscience MedicineClinical Trial Liaison ExperienceRegulatory Requirements UnderstandingGCP KnowledgeDrug Development ProcessesPatient Screening and Enrollment StrategiesScientific Support for Engagement DeliverablesAdverse Event ReportingProtocol Knowledge

Soft Skills

Strategic MindsetAttention to DetailNetworking SkillsCollaboration SkillsSelf-Motivation

Tools & Technologies

Digital PlatformsPresentation ToolsClinical Study Education Materials

Certifications & Qualifications

Valid Driver's License

Industry Keywords

Healthcare ProvidersPrincipal InvestigatorsKey Opinion Leaders (KOLs)Clinical ResearchField-Based Personnel

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Build peer-to-peer relationships with Principal Investigators and site staff in Neuroscience and Oncology
Provide protocol knowledge, address site enrollment barriers, and share clinical insights
Identify and develop relationships with KOLs, Principal Investigators, sub-investigators, and healthcare providers
Serve as the field-based scientific and clinical trial expert and advocate
Lead site engagement strategies to improve trial and site operational performance and enhance site relationships
Identify barriers to patient screening, enrollment, and retention at clinical sites
Collaborate with cross-functional stakeholders to develop and execute territory plans
Partner with internal teams and CROs to share insights and align site engagement activities
Communicate clinical and research issues and insights to clinical study teams and provide recommendations
Participate in clinical study education for healthcare professionals
Support sites through on-site presentations at healthcare institutions, conferences, and surrounding communities
Provide scientific support for site and patient engagement deliverables, including study-specific material development
Document and forward adverse event and product complaint reports according to Jazz policy
Adhere to relevant national and local Codes of Practice

Requirements

What you’ll need

Advanced degree (PharmD, MD, PhD or equivalent) with a minimum of 3 years of experience in oncology and/or neuroscience medicine, or License (RN, NP, CNP, PA or equivalent) with a minimum of a Master’s Degree (or equivalent) and a minimum of 5 years’ experience in oncology and/or neuroscience medicine
A minimum of 2 years of experience as a Medical Scientific Liaison (MSL), Clinical Scientist, Clinical Trial Liaison (CTL), or comparable field-based industry or clinical role
Strong strategic mindset and ability to research, critically analyze, and communicate complex scientific and medical information and data
Clear and concise communication and presentation skills
Excellent planning and organization skills, with high-level attention to detail and accuracy
Demonstrated interpersonal relationship building, networking, collaboration, and teamwork skills with HCPs and scientific and medical professionals
Ability to work autonomously and remain self-motivated
Ability to learn quickly, be flexible, and remain results-focused in a rapidly changing environment
Ability to influence without authority or gain acceptance/consensus in sensitive situations
Strong capabilities working with digital platforms and tools
Knowledge of target geographies, healthcare environments, and external experts in academia and the medical community
Well-established network and ability to develop trust and relationships with opinion leaders, PIs, clinical trial networks, and site research staff
Strong understanding of clinical trial methodology, GCP, drug development processes, and regulatory requirements
Understanding of regulatory and legal requirements for field-based personnel interacting with HCPs
Willingness to work outside normal work hours
Excellent command of written and spoken English
Willingness to travel up to 60% of the time
Valid driver’s license and residence in proximity to a major airport

Benefits

Comp & perks

Discretionary annual cash bonus or incentive compensation
Discretionary equity grants
Medical insurance
Dental insurance
Vision insurance
401k retirement savings plan
Flexible paid vacation