Skip to main content
Post your CV and find your next job on Indeed!

Research jobs in Brighton

Sort by: -
  • View similar jobs with this employer
    • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and…
    • 2+ years of hands-on experience in a quantitative role or research environment — such as data science, statistics, economics, finance, physics, biology,…
    • Improve & Evolve: Contribute to research standards, continuous improvement initiatives, and inclusive research practices.
  • View similar jobs with this employer
    • Identifying those items and pieces that would appeal to an online buyer.
    • A 25% discount on donated goods and 10% discount on New Goods in our shops.
    • Appraise the current market and educational research in the use of virtual and augmented reality and generative artificial intelligence and their use in…
    • Undertaking and completing tasks such as Root Cause Analysis, NC report writing or laboratory Hypothesis investigation in order to determine a suitable root…
    • Looking for part-time work in the Crawley area?
    • You will be assessing a variety of food, beverage, home & personal care products.
    • Experience across both public and private sector research.
    • Experience conducting research in complex public sector environments.
    • From styling windows with pre-loved fashion to talking with customers and making them feel welcome, volunteers are at the heart of our shop teams and every…
    • Within this role, you will provide R&D and Patent Box services to a range of clients from small start-ups to major multinationals across all lines of the sector…
    • Significant experience in quantitative consumer research methodologies.
    • Solid understanding of qual research: minimum requirement is knowing when to recommend…
    • Minimum 5 years of higher education with knowledge in market research and/or sensory research.
    • Experience in leading and mentoring research teams.
    • Developing and managing key study site documentation, such as Study Monitoring Plans, informed consent documents, source documents, patient instruction guides,…
    • Advance Diagnostics Innovation: Direct the operational aspects of companion diagnostics studies sponsored by external partners alongside early access and…
    • Develop Essential Documentation: Author and review key study site documents, including Study Monitoring Plans, informed consent forms, and case report forms,…

People also searched:

research assistant

Job Post Details

Clinical Research Associate - job post

IQVIA
3.7 out of 5 stars
Brighton
Full-time
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

Brighton

Full job description

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.

The Clinical Research Associate will support Oncology studies and cover sites across the UK

Apply today and forge a career with greater purpose, make an impact and never stop learning!

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
  • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Collaborate and liaise with study team members for project execution support as appropriate.

Requirements

  • Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.

  • In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

  • Life science degree educated or equivalent industry experience

  • Flexibility to travel to sites as required

*Please note - this role is not eligible for visa sponsorship*

IQVIA 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 worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Let Employers Find YouUpload Your Resume