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    • You will be responsible for the management of a range of external-facing projects, including clinical trials sponsored by pharmaceutical companies.
    • Create and maintain healthy and creative relationships with clinical trial sites and Principal Investigators, helping to support and influence where required.
    • Experience writing clinical study protocols and clinical study reports directly.
    • Lead all scientific elements of clinical studies from protocol development…
    • In-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management,…
    • Understanding of clinical trial protocols and report writing.
    • Support innovation and clinical process improvements.
    • 25 days’ holiday plus Bank Holidays.
    • The role will be part-time, (approx. 20 hrs per week) that can be arranged flexibly around other commitments and will be based within our office on West Street,…
    • We're looking for a Project Quality Manager who can build trusted relationships, bring people together and help teams consistently achieve high standards.
    • View all Laing O'Rourke jobs - Oxford jobs - Quality Manager jobs in Oxford
    • Salary Search: Project Quality Manager salaries in Oxford
    • Working closely with the University of Oxford, research partners, consultants, specialist subcontractors and internal delivery teams, you will help create a…
    • This role would suit someone with hands-on experience of clinical trials or research delivery who is confident working autonomously and supporting the…
    • In this role, you 'll become an expert in Vendor Management for global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study…
    • You have successfully managed multiple clinical trial protocols across diverse investigative sites.
    • Reading, United Kingdom | Full time | Home-based | R1530767.
    • Deep knowledge of clinical trial contract management processes.
    • Solid understanding of clinical trial regulations, GCP/ICH, and the overall drug development…
    • Reading, United Kingdom | Full time | Home-based | R1527743.
    • Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and…
    • Strong understanding of global clinical development, regulatory pathways, and therapeutic area dynamics.
    • This role is designed for a seasoned commercial leader…
    • Proven experience managing clinical trials end to end, from start-up through database lock and trial close-out.
    • Trial-level budget ownership and oversight.

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clinical research
Clinical Project Manager
234 Botley Road, Oxford OX2 0HP
£40,000 - £45,000 a year
Permanent, Full-time

Job details

Here’s how the job details align with your profile.

Pay

£40,000 - £45,000 a year

Job type

Permanent
Full-time

Benefits

Pulled from the full job description
Sick pay
Life insurance
Company pension
Private medical insurance
Cycle to work scheme

Full job description

A fantastic opportunity has become available for a Clinical Project Manager to join Caristo Diagnostics rapidly growing team. Based in Oxford, you will work in our global data operations team with colleagues in both U.S. and UK.

About Caristo Diagnostics

With the first and only FDA approved (July 29, 2026) coronary artery inflammation diagnostic medical device, CaRi-Heart®, Caristo Diagnostics is a global leader in AI technologies for cardiovascular disease, founded as a spin-out from the University of Oxford in 2018. Caristo also has an FDA approved (2025) coronary artery plaque diagnostic medical device. Its award-winning inflammation technology helps detect hidden heart disease and identify people at risk of a heart attack before symptoms appear allowing for proactive disease management. Working with leading hospitals, research institutions, and pharmaceutical partners, Caristo aims to save lives through early detection and personalized prevention. The company was named a 2026 Technology Pioneer by the World Economic Forum in June 2026. Learn more at www.caristo.com or follow Caristo on LinkedIn, YouTube, and X.

About the CaRi-Heart® Technology

Named first of “7 Technologies That Could Change Heart Healthcare Forevermore” by the Robb Report, the CaRi-Heart® technology is Caristo’s flagship offering which uncovers hidden coronary inflammation, a key driver of cardiovascular disease, on routine Coronary Computed Tomography Angiography (CCTA).

The technology is regulatory approved for clinical use in US, UK, Europe, and Australia and is in use with a growing number of hospitals and clinics. Multiple patents underpinning CaRi-Heart technologies have been granted in major jurisdictions around the world. In addition, exceptional validation results showing CaRi-Heart’s ability to aid the prediction of heart attacks have been published in leading medical journals including the Lancet, JACC, European Heart Journal, and Cardiovascular Research.

About The Role

Overview

Caristo is looking for a Clinical Project Manager to join their expanding Operations team. You will be responsible for the management of a range of external-facing projects, including clinical trials sponsored by pharmaceutical companies.

The ideal candidate will:

  • be motivated at the thought of working in an innovative healthcare start-up with a strong collaborative research and operations culture, helping to build a global business that will have material impact on the health and wellbeing of potentially millions of people.
  • share the company values of pushing the boundaries, taking ownership, caring for each other and acting with candour and professionalism.

JOB TITLE: Clinical Project Manager

DEPARTMENT: Operations

LOCATION: Oxford, UK

RESPONSIBILITIES:

Key Responsibilities include:

Management and administration of all aspects of clinical and pharma projects within Caristo’s Imaging Core Lab, including:

  • Strategies and direction to ensure project deliverables are completed within agreed cost, quality, timescale and scope boundaries.
  • Being the point of contact for communication with internal and external stakeholders.
  • Delivery of site training (remote).
  • Provide support to sites on medical imaging or data transfer related issues.
  • Develop or maintain trial/project-related SOP’s, protocols and other project-related documentation.
  • Development and maintenance of project plans using standard project management tools. ·
  • Development and maintenance of appropriate risk and issue registers for projects.
  • Use of metrics to assess the success of projects and make necessary changes.
  • Assist with responses on customers’ assessment and qualification processes.

SKILLS & EXPERIENCE REQUIRED

Essential

  • Bachelor or Masters’ degree in a relevant scientific discipline.
  • 2+ years’ experience of clinical project management within an industry (pharma/CRO) or academic setting.

Desirable

  • Proven success managing pharmaceutical projects and contracts within a Core Lab setting.
  • Experience of developing protocols and other documentation for research projects. · Experience managing medical imaging related projects.
  • Previous responsibility for Innovate UK, NIHR or Horizon 2020 grant management.
  • Experience working in a regulated medical devices environment.
  • Prior healthcare experience. Essential Soft Skills
  • Excellent analytical and problem-solving skills.
  • Strong attention to detail.
  • Excellent organisational and prioritisation skills.
  • Strong written and verbal communication skills.
  • Collaborative, adaptable, and customer-focused.

BENEFITS

  • Competitive salary
  • 25 holidays per year plus bank holidays
  • Enhanced pension contribution · Private medical insurance
  • Life insurance
  • Cycle-to-work scheme
  • Additional benefits for long-service

WHY JOIN CARISTO

  • Be part of a company at the cutting edge of medical technology, with the potential to save lives and revolutionise healthcare
  • Join a dynamic and growing team, with opportunities for personal and professional growth
  • Contribute to the development of groundbreaking products in a company poised for significant expansion
  • Enjoy a supportive and collaborative work environment, with a strong emphasis on innovation, quality, and impact

Caristo Diagnostics is committed to diversity and inclusion, and encourages applications from all qualified candidates, including those making a step up in their career. If you are passionate about making a difference in the world of medical imaging and meet the above criteria, we would love to hear from you.

Applicants should request our Candidate Privacy Notice for information as to how we will handle your personal data.

Pay: £40,000.00-£45,000.00 per year

Benefits:

  • Company pension
  • Cycle to work scheme
  • Private medical insurance
  • Sick pay

Application question(s):

  • What are your salary expectations?
  • Are you able to work in the office full tim?

Work authorisation:

  • United Kingdom (required)

Work Location: In person

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