Clinical Trial Liaison

Jazz Pharmaceuticals

. Build peer-to-peer relationships with Principal Investigators, site staff, key opinion leaders, sub-investigators, and healthcare providers in Neuroscience and Oncology .

Posted 11/4/2026full-timeRemote • United StatesMid-LevelSenior💰 $145,600 - $218,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Oncology and Neuroscience with a strong understanding of clinical trial methodology, regulatory requirements, and the drug development process. Proven ability to build relationships with healthcare professionals and lead site engagement strategies to enhance clinical trial performance.

Highest-signal resume keywords

Advanced Degree (PharmD, MD, PhD)Medical Scientific Liaison (MSL) ExperienceClinical Trial Methodology KnowledgeRegulatory Requirements UnderstandingStrong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial MethodologyOncology MedicineNeuroscience MedicineGCP ComplianceDrug Development ProcessAdverse Event ReportingScientific CommunicationPatient Engagement StrategiesStrategic ResearchCritical Analysis

Soft Skills

Interpersonal Relationship BuildingNetworkingCollaborationAttention to DetailFlexibility

Tools & Technologies

Digital PlatformsPresentation ToolsClinical Study Materials

Certifications & Qualifications

Valid Driver's License

Industry Keywords

Healthcare ProvidersPrincipal InvestigatorsClinical Trial SitesTarget Therapy AreasField-Based Personnel

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Build peer-to-peer relationships with Principal Investigators, site staff, key opinion leaders, sub-investigators, and healthcare providers in Neuroscience and Oncology
Serve as the field-based scientific and clinical trial expert regarding disease states, pipeline knowledge, and protocols
Lead site engagement strategies to improve trial and site operational performance
Identify barriers to patient screening, enrollment, and retention
Collaborate with cross-functional stakeholders and CRO partners to develop and execute territory plans
Communicate clinical and research issues and insights to clinical study teams
Participate in clinical study education for healthcare professionals around clinical trial sites
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 materials
Document and forward adverse event and product complaint reports according to company 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
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 understanding of clinical trial methodology, GCP, overall drug development process, and regulatory requirements
Understanding of regulatory and legal requirements for field-based personnel interacting with HCPs
Strong track record in target therapy areas and indications preferred
Willingness to travel up to 60% of the time
Valid driver’s license
Live in proximity of a major airport
Excellent command of written and spoken English
Strategic research, critical analysis, and communication of complex scientific and medical information
Clear and concise communication and presentation skills
Planning, organization, attention to detail, and accuracy
Interpersonal relationship building, networking, collaboration, and teamwork with HCPs and scientific and medical professionals
Ability to work autonomously, learn quickly, be flexible, and remain results-focused
Ability to influence without authority and gain acceptance or consensus in sensitive situations
Strong capabilities working with digital platforms and tools
Knowledge of target geographies, healthcare environments, and external experts
Established network and ability to develop trust with opinion leaders, PIs, clinical trial networks, and site research staff
Ability to work outside normal work hours as needed

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