Clinical Research Coordinator

1 month ago


Reading, Reading, United Kingdom ENGINEERINGUK Full time

Clinical Research Associate I Role Overview

Company Overview

ICON plc is a leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence.

Salary and Benefits

We offer a competitive salary of £45,000 - £55,000 per annum, depending on experience. In addition to your base salary, you can expect a range of benefits, including:

  • An annual leave entitlement of 25 days, plus bank holidays
  • A range of health insurance options to suit your needs
  • Competitive retirement planning offerings
  • A Global Employee Assistance Programme (EAP)
Job Description

We are seeking a Clinical Research Associate to join our diverse team in the UK. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

  1. You will work independently to coordinate all activities for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation.
  2. You will ensure patient safety by adhering to ICON's procedures, protocols, and regulatory requirements.
Required Skills and Qualifications

To succeed in this role, you will need:

  • A university degree in medicine, science, or a related field
  • Knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data
  • Excellent written and verbal communication skills in English
  • A valid driver's license and willingness to travel at least 60% of the time (international and domestic)
Benefits and Career Development

Our success depends on the quality of our people. We offer a range of benefits to support your well-being and career development, including:

  • Opportunities for professional growth and development
  • A supportive and inclusive work environment
  • A comprehensive benefits package


  • Reading, Reading, United Kingdom Pharmiweb Full time

    Pharmiweb is a leading global provider of clinical research services. We are seeking a Research Operations Coordinator to join our sponsor-dedicated team and support sites across the South West of England.About the RoleThe Research Operations Coordinator will be responsible for providing administrative support to the clinical study team, including...


  • Reading, Reading, United Kingdom ICON plc Full time

    Clinical Research Administrator - UK, ReadingICON plc is a world-leading healthcare intelligence and clinical research organization.We are seeking a Clinical Research Associate to join our team at ICON Plc.Job Description:Coordinate all activities for setting up and monitoring clinical trials, ensuring compliance with regulations.Collect and analyze critical...


  • Reading, Reading, United Kingdom ICON plc Full time

    Based in the UK, ICON plc is a world-leading healthcare intelligence and clinical research organization.We are seeking a Clinical Research Associate to join our diverse team at ICON Plc. As a key member of our research department, you will oversee and coordinate clinical trials, ensuring compliance with regulations and collecting critical data.Key...


  • Reading, Reading, United Kingdom ICON Full time

    Company Overview:ICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to fostering an inclusive environment driving innovation and excellence. We are seeking a Clinical Research Associate to join our dynamic team at ICON Plc in Reading, UK.Salary:The estimated salary for this role is £45,000 - £60,000 per annum,...


  • Reading, Reading, United Kingdom ENGINEERINGUK Full time

    Clinical Research Administrator Role at ICON plcEngineer clinical trials to shape the future of healthcare with us.About UsWe are a leading provider of healthcare intelligence and clinical research services. Our mission is to foster an inclusive environment driving innovation and excellence, while delivering exceptional results for our clients.The...


  • Reading, Reading, United Kingdom ICON Full time

    Clinical trials coordinators play a vital role in ensuring the success of clinical trials at ICON. As a senior proposal developer, you will be responsible for developing and coordinating proposals and budgets for new business opportunities.About the CompanyICON is a world-leading healthcare intelligence and clinical research organization. We pride ourselves...


  • Reading, Reading, United Kingdom ICON plc Full time

    At ICON plc, we are seeking an experienced Clinical Research Project Manager to join our EU-based team. As a key member of our Global RWE late phase project management team, you will contribute towards a culture of business excellence with a focus on quality, scope, timelines, and adding value to the business.The successful candidate will have demonstrable...


  • Reading, Reading, United Kingdom ENGINEERINGUK Full time

    Clinical Research AdministratorCompany OverviewICON plc is a world-leading healthcare intelligence and clinical research organization.Job SummaryWe are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc.Key Responsibilities:Coordinate all activities for setting up and monitoring a study, complete accurate study...


  • Reading, Reading, United Kingdom ICON plc Full time

    Job DescriptionWe are seeking a skilled Clinical Research Data Manager to join our team at ICON plc. As a key member of our clinical research systems and reporting team, you will play a critical role in managing and optimizing our data management processes.Your Responsibilities:Manage and optimize clinical research systems to ensure they meet the needs of...


  • Reading, Reading, United Kingdom IQVIA Full time

    We are seeking a skilled Clinical Research Professional to join our sponsor-dedicated team. Located in Northern England and Scotland, this role offers an excellent opportunity for CRAs looking to grow their career.About the RoleAs a Clinical Research Professional, you will be responsible for performing site monitoring visits, adapting and driving subject...


  • Reading, Reading, United Kingdom IQVIA LLC Full time

    Clinical Research Associate RoleWe are seeking a skilled Clinical Research Associate to support our sponsor-dedicated team in the South West England region.This is an excellent opportunity for CRAs local to the area who would value:Collaborative teams and supportive leadershipA variety of career opportunities to grow with usTechnology-enabled resources for...


  • Reading, Reading, United Kingdom IQVIA Full time

    We are currently seeking a Clinical Trials Coordinator Lead to join our team in the South West of England. In this role, you will be responsible for managing the progress of assigned studies, tracking regulatory submissions and approvals, and resolving data queries.About IQVIAIQVIA is a global leader in clinical research services, commercial insights, and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    IQVIA, Inc. is seeking a Clinical Research Professional to join our team. As a Clinical Research Professional, you will be responsible for performing site monitoring visits and working with sites to adapt, drive, and track subject recruitment plans.The ideal candidate will have a life science degree education and independent on-site monitoring experience....


  • Reading, Reading, United Kingdom IQVIA LLC Full time

    Seeking a talented Clinical Research Associate to support our team in the South West of England. This role offers an exciting opportunity for CRAs who value supportive leadership, collaborative teams, and technology-enabled resources.The successful candidate will be responsible for conducting site monitoring visits, adapting subject recruitment plans,...


  • Reading, Reading, United Kingdom IQVIA Argentina Full time

    Clinical Research Data ManagerWe are looking for an experienced Clinical Research Data Manager to lead our data integration efforts at IQVIA Argentina. In this role, you will oversee the acquisition, processing, and analysis of external data to support clinical trials.About the RoleDesign and implement data integration strategies to meet clinical trial...


  • Reading, Reading, United Kingdom Intuitive Full time

    Job DescriptionWe are seeking a highly skilled Clinical Project Manager to join our team in the Clinical Affairs Department. The ideal candidate will have experience working in the medical device industry, with a strong background in clinical affairs and research functions.The purpose of this job function is to oversee the initiation, progress, and conduct...


  • Reading, Reading, United Kingdom Royal Berkshire NHS Foundation Trust Full time

    The Royal Berkshire NHS Foundation Trust is seeking a highly skilled Clinical Research Nurse to lead the delivery of high-quality care to research participants and their families.Job OverviewThis Band 6 position requires a dedicated professional with a passion for research and excellent leadership skills.Main ResponsibilitiesManage resources effectively to...


  • Reading, Reading, United Kingdom Royal Berkshire NHS Foundation Trust Full time

    We are seeking a highly skilled Clinical Research Team Lead to join our team at the Royal Berkshire NHS Foundation Trust. As a key member of our clinical research team, you will be responsible for leading the development of R&D strategies, policies, and plans to build capacity for research within and across the Trust.Main Responsibilities:Develop and...


  • Reading, Reading, United Kingdom IQVIA, Inc. Full time

    Company Overview">IQVIA, Inc. is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health...


  • Reading, Reading, United Kingdom IQVIA Full time

    Job Title:Clinical Research Associate LeadAbout the Role:IQVIA UK is seeking an experienced Clinical Research Associate Lead to strengthen our cFSP team. The successful candidate will be responsible for performing site monitoring visits, adapting and driving subject recruitment plans, and managing study sites to ensure compliance with Good Clinical Practice...