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Biomedical Scientist jobs in West Berkshire

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    • ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
    • View all ICON Plc jobs - Reading jobs
    • Salary Search: Clinical Research Associate salaries in Reading
    • See popular questions & answers about ICON Plc
    • As a PK Scientist at ICON, you will be responsible for designing and conduct pharmacokinetic (PK) studies to evaluate drug absorption, distribution, metabolism,…
    • Provide strategic leadership and demonstrating accountability for the clinical programs supporting early clinical development and clinical pharmacology.
    • As an CSA at ICON, you will play a pivotal role in supporting clinical trial operations by ensuring site compliance, documentation accuracy, and readiness for…
    • In RSSL we are customer focused, science led and results driven.
    • The RSSL Microbiology laboratory performs a wide range of analytical analyses for a variety of…
    • To facilitate process development and validation activities, including technical support and oversight for external cell line development, cell banking and…
    • We're looking for a clinical scientist — someone who has been the scientific lead for clinical studies before, from protocol development to start-up (…
    • The Cardiovascular Program Specialist (CVPS) will provide expert clinical support, education, and training to physicians, nurses, and hospital staff on the use…
    • In addition, exceptional validation results showing CaRi-Heart’s ability to aid the prediction of heart attacks have been published in leading medical journals…
    • You will also have the opportunity to oversee contract research organisations (CROs) that conduct in vivo studies of our immunotherapy candidates.
    • Reading, United Kingdom | Full time | Field-based | R1510425.
    • IQVIA has access to significant data pools allowing better site selection and recruitment.
    • Reading, United Kingdom | Full time | Home-based | R1562059.
    • Serve as primary point of contact for customer on data management deliverables.
    • Team Leadership: Mentor and build a team of experienced and burgeoning scientists, guiding them in COA methodologies and scientific best practices.
    • A substantial part of the role will focus on FreeGSNKE, UKAEA’s open-source tool for modelling tokamak plasma equilibria and evolution.
    • The team currently consists of controls engineers, microbiologists, a chemist, mechanical design engineers, an analysis engineer, one test and development…

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Clinical Research Associate
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Full job description

CRAII - Oncology UK

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.



As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.



Oncology Clinical Research Associate (All Levels) – UK South-West

Join ICON's FSP Team

ICON's Functional Service Provision (FSP) team is growing, and we're seeking Oncology Clinical Research Associates at all levels to join a dedicated partnership with a long-standing global biopharmaceutical leader.

This is an exciting opportunity to play a key role in advancing innovative oncology research while working within a collaborative, supportive, and highly experienced clinical team. You'll be responsible for overseeing site performance, ensuring data quality and patient safety, and helping to deliver clinical studies that have the potential to improve patients' lives.

What You'll Be Doing

  • Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
  • Conduct on-site visits across the South West UK region, supporting study sites and identifying solutions to operational challenges.
  • Partner with cross-functional teams to ensure accurate, timely collection and reporting of study data.
  • Build and maintain strong working relationships with investigators, site staff, and other key stakeholders.
  • Provide guidance and support to site personnel, helping to ensure the successful delivery of clinical trials.

What We're Looking For

  • A degree in Life Sciences, Nursing, Medicine, or a related discipline.
  • Previous UK experience as a Clinical Research Associate within oncology studies.
  • Strong understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice (GCP).
  • Excellent organisational skills, with the ability to manage multiple sites and priorities effectively.
  • Proven experience in site management, monitoring activities, and ensuring high-quality study delivery.
  • Strong communication and relationship-building skills.
  • Willingness and ability to travel to sites across the UK, with a valid driving licence.

Interested?

If your experience aligns with the above, we'd love to hear from you. Apply today and a member of our recruitment team will be in touch to arrange an informal conversation and discuss the opportunity in more detail.



Employment with ICON is contingent upon having the legal right to work in the country where the role is based.



Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.



Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.



Visit our careers site to read more about the benefits ICON offers.



Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.



If you require reasonable accommodations during the recruitment process, please let us know or submit a request .

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