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Clinical Trials jobs in Surrey Heath

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    • Familiarity with clinical trial regulations and Good Clinical Practice (GCP) guidelines is advantageous but not essential.
    • Must hold a valid NMC registration.*.
    • Knowledge of GCP guidelines and regulatory requirements pertinent to clinical trials.
    • The successful candidate will be responsible for overseeing and…
    • Experience writing clinical study protocols and clinical study reports directly.
    • Lead all scientific elements of clinical studies from protocol development…
    • The Alzheimer's Society UKDTN Lead Clinical Research Nurse is a senior clinical leadership role responsible for leading the delivery and development of early…
    • View all Surrey and Borders Partnership NHS Foundation Trust jobs - Chertsey jobs - Research Nurse jobs in Chertsey
    • Salary Search: ALZHEIMER’S SOCIETY UKDTN LEAD CLINICAL RESEARCH NURSE salaries in Chertsey
    • See popular questions & answers about Surrey and Borders Partnership NHS Foundation Trust
    • Reading, United Kingdom | Full time | Home-based | R1513972.
    • This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized…
    • 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,…
    • CSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line of code to final submission package.
    • As an Alzheimer's Society UKDTN Senior Clinical Research Nurse, the post holder will provide clinical and administrative support to ensure effective delivery of…
    • 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…
    • Minimum of 8 years of experience in clinical trial statistics, preferably within a pharmaceutical or CRO setting.
    •  Study Design and Strategy:
    • 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 Nurse
Desborough Road, High Wycombe HP11 2QW
£40,000 - £50,000 a year
Temporary, Full-time

Job details

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

Pay

£40,000 - £50,000 a year

Job type

Temporary
Full-time

Benefits

Pulled from the full job description
Free parking
Additional leave
Health & wellbeing programme
Company events
On-site parking

Full job description

Job Overview

No experience necessary, would suit a nurse looking to break into clinical research!!

Must hold a valid NMC registration.

Temporary Role for 8 week with potential to be extended

. The ideal candidate will play a crucial role in the management and execution of clinical trials, ensuring the highest standards of patient care while contributing to vital medical research. This position requires a strong background in nursing, with a particular emphasis on patient interaction and an understanding of human anatomy.

Duties

  • Conduct patient assessments and monitor their health status throughout the research study.
  • Administer medications and treatments as per study protocols while ensuring patient safety and comfort.
  • Collect and document data accurately, maintaining meticulous records for compliance with regulatory requirements.
  • Collaborate with physicians, researchers, and other healthcare professionals to facilitate effective study implementation.
  • Educate patients about the study procedures, potential risks, and benefits, ensuring informed consent is obtained.
  • Participate in the development of research protocols and assist in the preparation of reports for regulatory submissions.
  • Maintain confidentiality of patient information in accordance with ethical guidelines and organisational policies.

Requirements

  • Registered Nurse (RN) qualification with a current nursing licence.
  • Proven experience in patient care, preferably within a research or clinical setting.
  • Strong knowledge of human anatomy and physiology to effectively assess patient conditions.
  • Excellent communication skills, both verbal and written, to interact with patients and team members effectively.
  • Ability to work independently as well as part of a multidisciplinary team.
  • Strong organisational skills with attention to detail for accurate data collection and documentation.
  • Familiarity with clinical trial regulations and Good Clinical Practice (GCP) guidelines is advantageous but not essential.

If you are passionate about advancing medical knowledge through research while providing exceptional care to patients, we encourage you to apply for this rewarding opportunity as a Research Nurse.

Pay: £40,000.00-£50,000.00 per year

Benefits:

  • Additional leave
  • Company events
  • Free parking
  • Health & wellbeing programme
  • On-site parking

Application question(s):

  • How many years of clinical research experience do you have?

Experience:

  • Nursing: 1 year (required)
  • Clinical research: 1 year (required)

Licence/Certification:

  • NMC (required)

Work Location: In person

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