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Director, Clinical Trial Feasibility & Site Intelligence

Jazz Pharmaceuticals
Jazz Pharmaceuticals
5-15 years
$189,600 – $284,400
10 Jan. 12, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Director, Clinical Trial Feasibility & Site Intelligence | Jazz Pharmaceuticals

Locations: London, UK; Philadelphia, PA, USA (Remote / Home-Based Options)
Category: Research & Development
Employment Type: Full-Time, Regular
Req ID: R010805
Salary Range (US): $189,600 – $284,400 base, plus potential bonus & equity


About Jazz Pharmaceuticals

Jazz Pharmaceuticals is a global biopharma company committed to transforming the lives of patients and families through innovative therapies. Our portfolio spans sleep disorders, epilepsy, oncology, and neuroscience, with a strong focus on delivering treatments for serious diseases with limited or no therapeutic options. With headquarters in Dublin, Ireland, Jazz operates globally, driving pioneering research and development while ensuring patient-centered outcomes.

For more information, visit: www.jazzpharmaceuticals.com


Role Overview

The Director of Clinical Trial Feasibility & Site Intelligence leads the strategy, design, and execution of global clinical trial feasibility and site intelligence initiatives. This senior leadership role is critical in optimizing protocol design, site selection, country feasibility, and study placement strategies through data-driven insights, advanced analytics, and cross-functional collaboration.

This role ensures that Jazz clinical trials are efficient, scalable, and patient-centric, while leveraging historical data, real-world evidence, AI/ML tools, and predictive analytics to inform decision-making.


Key Responsibilities

  • Provide strategic leadership for the global feasibility and site intelligence function.

  • Develop and oversee processes to optimize study timelines, budgets, and operational planning through robust site and country feasibility assessment.

  • Deliver actionable feasibility insights and site placement strategies to support clinical trial design and execution.

  • Lead site identification, selection, and enrolment optimization initiatives across multiple therapeutic areas.

  • Integrate historical, real-world, and AI-driven data to improve feasibility accuracy, reduce operational risk, and optimize trial outcomes.

  • Evaluate and implement cutting-edge tools, vendors, and processes to enhance feasibility planning, ROI, and trial efficiency.

  • Establish and monitor KPIs and operational metrics for site and country performance across studies.

  • Provide cross-functional leadership, collaborating with Clinical Operations, Clinical Development, and Medical Affairs to embed feasibility insights into study strategies.

  • Manage and develop a high-performing team, including hiring, coaching, and resource planning.

  • Oversee CRO and vendor partnerships, ensuring governance, performance management, and contract compliance.

  • Serve as a Subject Matter Expert (SME) on feasibility, site intelligence, and enrolment optimization, both internally and externally.


Required Qualifications & Skills

  • Education: Bachelor’s degree in Life Sciences or related field required; advanced degree preferred.

  • Experience:

    • Minimum 15 years in clinical research, including 5+ years in leadership roles within feasibility or site intelligence.

    • Proven success in strategic leadership of global clinical trial feasibility and site intelligence.

    • Expertise in data-driven site selection, operational planning, and enrolment modeling.

    • Experience leveraging historical and real-world data, AI/ML tools, EMR/claims data, geo-mapping, and patient registries to inform study design.

  • Demonstrated ability to lead high-performing teams, manage complex projects, and drive cross-functional decisions.

  • Experience managing vendors, budgets, and ROI for feasibility initiatives.

  • Familiarity with inspection readiness, process improvement, and regulatory compliance.


Why Join Jazz Pharmaceuticals

  • Lead innovative, data-driven feasibility strategies impacting global clinical trials.

  • Collaborate across therapeutic areas and international markets to optimize patient-centric study design.

  • Competitive compensation, including base pay, discretionary bonus, and potential equity awards.

  • Comprehensive benefits package including medical, dental, vision, retirement plans, and flexible paid vacation.

  • Opportunity to contribute to transformative therapies improving patient outcomes worldwide.

EEO Statement:
Jazz Pharmaceuticals is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, disability, veteran status, or other protected characteristics.