Associate director, clinical trial feasibility & site identification - oncology in Slough

Associate director, clinical trial feasibility & site identification - oncology in Slough

Slough Full-Time 130000 - 195000 £ / year (est.) Home office (partial)
Jazz Pharmaceuticals

At a Glance

  • Tasks: Lead innovative oncology clinical trial planning and site selection using data-driven insights.
  • Company: Join Jazz Pharmaceuticals, a global biopharma leader transforming patient lives.
  • Benefits: Competitive salary, bonuses, flexible vacation, and comprehensive health benefits.
  • Other info: Remote work opportunity with excellent career growth and a culture of inclusion.
  • Why this job: Make a real impact in oncology research while collaborating with diverse teams.
  • Qualifications: 8-10 years in clinical research, with expertise in feasibility and site intelligence.

The predicted salary is between 130000 - 195000 £ per year.

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide.

The Associate Director, Clinical Trial Feasibility & Site Intelligence - Oncology, is responsible for providing advanced expertise in feasibility and site intelligence processes to inform clinical trial planning and execution across the Jazz clinical trial portfolio. The role leverages cross-functional collaboration, analytics, and data-driven insights—both historical and predictive—to inform protocol design, country and site selection, and enrollment planning. This individual will contribute feasibility insights and study placement strategies to support clinical study design and planning. The role requires a strong ability to integrate data sources and expertise to deliver robust study scenarios, enhancing country and site selection with focused expertise in oncology clinical trials. This position is critical to ensuring efficient, data-driven, and scalable clinical trial planning strategies, but does not include direct management of colleagues.

Essential Functions/Responsibilities

  • Subject matter expert in oncology global clinical trial feasibility and site intelligence to support operational planning and study design.
  • Serve as a portfolio level Subject Matter Expert (SME) on feasibility assessment, enrollment optimization, and site intelligence both internally and in relevant industry discussions.
  • Partner cross-functionally to deliver feasibility insights and study placement strategies that inform protocol design, timelines, and enrollment projections.
  • Develop program or study scenarios and plans through data-driven assessment of country and site footprint, enrollment rate, and site activation projections.
  • Lead site identification and selection activities at indication, program or study level by collaborating with study teams to define strategies aligned with protocol requirements.
  • Functional oversight of CRO and vendors supporting feasibility, including performance management, contract and budget management.
  • Leverage historical and predictive data, real-world evidence, and emerging technologies to optimize protocol design and mitigate operational risks.
  • Identify and evaluate feasibility tools, vendors, and approaches; provide input on their impact on cost, speed, diversity, and data quality.
  • Contribute to the definition and monitoring of KPIs and operational metrics for country and site performance; use insights to recommend process improvements.
  • Act as a trusted partner to Clinical Operations, Clinical Development, Medical Affairs, GPSE and other stakeholders to ensure feasibility insights are embedded into study execution strategies.

Required Knowledge, Skills, and Abilities

  • Demonstrated expertise in global feasibility assessment, enrollment modeling, and data-driven site selection.
  • Experience leveraging real-world data sources and digital technologies (e.g., EMR/claims data, AI/ML, geo-mapping, registries) to inform study planning.
  • Proven ability to influence cross-functional decision-making through data-driven insights.
  • Strong understanding of vendor evaluation and collaboration related to feasibility and site intelligence.
  • Experience functional oversight of vendors and CROs in feasibility data analysis.
  • Experience contributing to inspection readiness and continuous process improvement initiatives.
  • Excellent organizational, communication, and teamwork skills with the ability to build effective partnerships across external vendors, internal functions, and regions.

Required/Preferred Education and Licenses

  • Bachelor’s degree in life sciences, healthcare, or related field required; advanced degree preferred.
  • 8–10 years of experience in clinical research, with at least 5 years specifically in clinical trial feasibility or site intelligence.

Associate director, clinical trial feasibility & site identification - oncology in Slough employer: Jazz Pharmaceuticals

Jazz Pharmaceuticals is an exceptional employer, offering a dynamic work culture that prioritises collaboration, inclusion, and personal growth. With a strong commitment to employee development and a focus on innovative research in oncology, employees benefit from competitive compensation packages, comprehensive health benefits, and opportunities for professional advancement in a supportive environment. Located in Dublin, Ireland, Jazz fosters a sense of belonging and empowers its team members to make a meaningful impact on patients' lives worldwide.

Jazz Pharmaceuticals

Contact Details:

Jazz Pharmaceuticals Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Associate director, clinical trial feasibility & site identification - oncology in Slough

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We think you need these skills to ace Associate director, clinical trial feasibility & site identification - oncology in Slough

Oncology Clinical Trial Feasibility
Site Intelligence
Data-Driven Insights
Cross-Functional Collaboration
Enrollment Optimization
Feasibility Assessment
Vendor Management

Some tips for your application 🫡

Show Off Your Lab Skills:In the biotechnology field, it's super important to highlight your lab experience in your CV. Be sure to mention specific techniques or instruments you've mastered (think PCR, gel electrophoresis, etc.) and any relevant projects you've worked on. This will show Jazz Pharmaceuticals that you have the hands-on skills they need.

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Craft a Compelling Cover Letter:Since this is a full-time role, your cover letter should reflect not only your passion for biotechnology but also your long-term career ambitions. Share why you're excited about the work that Jazz Pharmaceuticals does and how you envision contributing to their goals. This shows that you’re not just looking for any job, but you're genuinely invested in this opportunity.

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How to prepare for a job interview at Jazz Pharmaceuticals

Brush Up on Lab Techniques

Since you're eyeing a full-time gig in biotechnology, make sure you're well-versed in the lab techniques relevant to the role. Be ready to talk about PCR, CRISPR, or any specific methods mentioned in the job description at Jazz Pharmaceuticals. You might even be asked to demonstrate your understanding of these processes.

Know Your Bioinformatics Tools

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Research Recent Biotech Innovations

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