Clinical Trial Liaison

Jazz Pharmaceuticals • Philadelphia, PA

1d • Remote

About The Position

The Clinical Trial Liaison (CTL) is a field-based scientific expert who supports and accelerates clinical trial execution in Neuroscience, Oncology, and Neuro-oncology. The role builds peer-to-peer relationships with Principal Investigators and clinical site staff, provides protocol and disease-state expertise, identifies barriers to trial participation, and shares clinical insights to improve site engagement and trial performance.

The CTL works with internal cross-functional stakeholders and CRO partners to plan and carry out site engagement activities, communicate research-site insights to clinical study teams, and support clinical education and engagement materials. The position requires travel up to 60% of the time, comfort working outside normal work hours as business demands require, a valid driver’s license, and residence near a major airport.

Requirements

• Advanced degree (PharmD, MD, PhD, or equivalent) and at least 3 years of experience in oncology and/or neuroscience medicine; alternatively, a license (RN, NP, CNP, PA, or equivalent), at least a master’s degree or equivalent, and at least 5 years of experience in oncology and/or neuroscience medicine.
• At least 2 years of experience as an MSL, Clinical Scientist, CTL, or in a comparable field-based industry or clinical role.
• Strategic mindset and ability to research, critically analyze, and communicate complex scientific and medical information and integrate it into site engagement plans and activities.
• Clear, concise communication and presentation skills.
• Excellent planning and organization skills, with close attention to detail and accuracy.
• Interpersonal relationship-building, networking, collaboration, and teamwork skills, particularly with healthcare professionals and leading scientific and medical professionals.
• Self-motivation and ability to work autonomously.
• Ability to learn quickly, remain flexible, and focus on results in a rapidly changing environment.
• Ability to influence without authority or gain acceptance and consensus in sensitive situations while preserving relationships.
• Strong capabilities with digital platforms and tools.
• Knowledge of target geographies, healthcare environments, and external experts in academia and the medical community.
• Established network and demonstrated ability to develop trust and relationships with opinion leaders, Principal Investigators, clinical trial networks, and site research staff in relevant disease states.
• Strong understanding of clinical trial methodology, GCP, drug development, and applicable regulatory requirements, including legal and regulatory requirements for field-based personnel interacting with healthcare professionals.
• Comfort working outside normal work hours to meet business demands.
• Excellent 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.

Nice To Haves

• Strong track record and demonstrated success in target therapy areas and indications, such as targeted therapies for solid tumors or epilepsy.

Responsibilities

• Build peer-to-peer relationships with key opinion leaders, Principal Investigators, sub-investigators, and healthcare providers in target therapeutic areas and select pipeline indications.
• Serve as a field-based scientific and clinical trial expert, engaging Principal Investigators and site staff in protocol-related discussions using disease-state and pipeline knowledge.
• Lead site engagement strategies to improve trial and site operational performance and strengthen site relationships.
• Identify barriers to patient screening, enrollment, and retention at clinical sites and work to address them.
• Collaborate with cross-functional stakeholders to develop and execute territory plans aligned with site engagement objectives and deliverables.
• Partner with CROs to share insights and coordinate site engagement activities without duplicating efforts.
• Communicate clinical and research issues and insights from sites and healthcare providers to clinical study teams, and provide recommendations and creative solutions as appropriate.
• Participate in clinical study education for healthcare professionals in communities around clinical trial sites.
• Support sites through presentations at healthcare institutions, conferences, and surrounding communities.
• Provide scientific support for site and patient engagement deliverables, including development of site- and patient-facing study materials.
• Document and forward reports of adverse events and product complaints according to company policy.
• Adhere to relevant national and local Codes of Practice.

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• 401(k) retirement savings plan
• Flexible paid vacation
• May be eligible for a discretionary annual cash bonus or incentive compensation, depending on the role
• May be eligible for discretionary equity grants

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level